Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
7,522
archived clinical trials in
Chronic Pain

Cryotherapy in Preventing Peripheral Neuropathy and Nail Toxicity in Patients With Breast Cancer Who Are Receiving Paclitaxel
Cold Therapy to Prevent Paclitaxel-Induced Peripheral Neuropathy and Cutaneous Toxicity
Status: Enrolling
Updated:  1/9/2018
mi
from
Chicago, IL
Cryotherapy in Preventing Peripheral Neuropathy and Nail Toxicity in Patients With Breast Cancer Who Are Receiving Paclitaxel
Cold Therapy to Prevent Paclitaxel-Induced Peripheral Neuropathy and Cutaneous Toxicity
Status: Enrolling
Updated: 1/9/2018
Northwestern University
mi
from
Chicago, IL
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Reducing Operative and Post-operative Morbidity in Living Kidney Donors With the Airseal System
Reducing Operative and Post-operative Morbidity in Living Kidney Donors With the Airseal System: A Randomized Control Trial
Status: Enrolling
Updated:  1/12/2018
mi
from
New Haven, CT
Reducing Operative and Post-operative Morbidity in Living Kidney Donors With the Airseal System
Reducing Operative and Post-operative Morbidity in Living Kidney Donors With the Airseal System: A Randomized Control Trial
Status: Enrolling
Updated: 1/12/2018
Yale New Haven Transplantation Center
mi
from
New Haven, CT
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A Study of Sternal Closure After Open Heart Surgery: Rigid Versus Wire Closure
A Prospective Randomized Study of Two Types of Sternal Closure After Open Heart Surgery: Rigid Sternal Fixation vs. Sternal Wire Closure
Status: Enrolling
Updated:  1/16/2018
mi
from
Philadelphia, PA
A Study of Sternal Closure After Open Heart Surgery: Rigid Versus Wire Closure
A Prospective Randomized Study of Two Types of Sternal Closure After Open Heart Surgery: Rigid Sternal Fixation vs. Sternal Wire Closure
Status: Enrolling
Updated: 1/16/2018
Thomas Jefferson University Hospital
mi
from
Philadelphia, PA
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Telehealth Outreach for Chronic Back Pain
Telehealth Outreach for Chronic Back Pain
Status: Enrolling
Updated:  1/16/2018
mi
from
San Diego, CA
Telehealth Outreach for Chronic Back Pain
Telehealth Outreach for Chronic Back Pain
Status: Enrolling
Updated: 1/16/2018
VA San Diego Healthcare System, San Diego
mi
from
San Diego, CA
Click here to add this to my saved trials
Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain
A Prospective, Randomized-Controlled, Multicenter Study Evaluating Primary Plating in High-Risk Median Sternotomy Patients for Osteosynthesis and Pain
Status: Enrolling
Updated:  1/16/2018
mi
from
Phoenix, AZ
Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain
A Prospective, Randomized-Controlled, Multicenter Study Evaluating Primary Plating in High-Risk Median Sternotomy Patients for Osteosynthesis and Pain
Status: Enrolling
Updated: 1/16/2018
St. Joseph's Heart and Lung Institute
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain
A Prospective, Randomized-Controlled, Multicenter Study Evaluating Primary Plating in High-Risk Median Sternotomy Patients for Osteosynthesis and Pain
Status: Enrolling
Updated:  1/16/2018
mi
from
Sacramento, CA
Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain
A Prospective, Randomized-Controlled, Multicenter Study Evaluating Primary Plating in High-Risk Median Sternotomy Patients for Osteosynthesis and Pain
Status: Enrolling
Updated: 1/16/2018
University of California, Davis Medical Center
mi
from
Sacramento, CA
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Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain
A Prospective, Randomized-Controlled, Multicenter Study Evaluating Primary Plating in High-Risk Median Sternotomy Patients for Osteosynthesis and Pain
Status: Enrolling
Updated:  1/16/2018
mi
from
Chicago, IL
Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain
A Prospective, Randomized-Controlled, Multicenter Study Evaluating Primary Plating in High-Risk Median Sternotomy Patients for Osteosynthesis and Pain
Status: Enrolling
Updated: 1/16/2018
University of Chicago
mi
from
Chicago, IL
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Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain
A Prospective, Randomized-Controlled, Multicenter Study Evaluating Primary Plating in High-Risk Median Sternotomy Patients for Osteosynthesis and Pain
Status: Enrolling
Updated:  1/16/2018
mi
from
Memphis, TN
Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain
A Prospective, Randomized-Controlled, Multicenter Study Evaluating Primary Plating in High-Risk Median Sternotomy Patients for Osteosynthesis and Pain
Status: Enrolling
Updated: 1/16/2018
Baptist Memorial Hospital
mi
from
Memphis, TN
Click here to add this to my saved trials
Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain
A Prospective, Randomized-Controlled, Multicenter Study Evaluating Primary Plating in High-Risk Median Sternotomy Patients for Osteosynthesis and Pain
Status: Enrolling
Updated:  1/16/2018
mi
from
Temple, TX
Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain
A Prospective, Randomized-Controlled, Multicenter Study Evaluating Primary Plating in High-Risk Median Sternotomy Patients for Osteosynthesis and Pain
Status: Enrolling
Updated: 1/16/2018
Scott & White Memorial Hospital
mi
from
Temple, TX
Click here to add this to my saved trials
Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain
A Prospective, Randomized-Controlled, Multicenter Study Evaluating Primary Plating in High-Risk Median Sternotomy Patients for Osteosynthesis and Pain
Status: Enrolling
Updated:  1/16/2018
mi
from
Leipzig,
Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain
A Prospective, Randomized-Controlled, Multicenter Study Evaluating Primary Plating in High-Risk Median Sternotomy Patients for Osteosynthesis and Pain
Status: Enrolling
Updated: 1/16/2018
Leipzig Heart Center
mi
from
Leipzig,
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Effectiveness Trial for Evaluating IAHA for PFPS
A Randomized, Pragmatic, Effectiveness Trial Evaluating Intra-articular Hyaluronan for the Symptomatic Treatment of Chronic Patellofemoral Pain Syndrome
Status: Enrolling
Updated:  1/18/2018
mi
from
New York, NY
Effectiveness Trial for Evaluating IAHA for PFPS
A Randomized, Pragmatic, Effectiveness Trial Evaluating Intra-articular Hyaluronan for the Symptomatic Treatment of Chronic Patellofemoral Pain Syndrome
Status: Enrolling
Updated: 1/18/2018
Center for Musculoskeletal Care - NYU Langone Medical Center
mi
from
New York, NY
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Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
Phoenix, AZ
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated: 1/19/2018
Maricopa Integrated Health System
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
Little Rock, AR
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated: 1/19/2018
Arkansas Children's Hospital
mi
from
Little Rock, AR
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Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
Stanford, CA
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated: 1/19/2018
Stanford Univ Med Ctr
mi
from
Stanford, CA
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Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
New Haven, CT
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated: 1/19/2018
Yale-New Haven Children's Hospital
mi
from
New Haven, CT
Click here to add this to my saved trials
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
Washington,
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated: 1/19/2018
Childrens National Medical Center
mi
from
Washington,
Click here to add this to my saved trials
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
Detroit, MI
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated: 1/19/2018
Children's Hospital of Michigan
mi
from
Detroit, MI
Click here to add this to my saved trials
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
Akron, OH
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated: 1/19/2018
Children's Hospital Medical Center of Akron d/b/a Akron Children's Hospital
mi
from
Akron, OH
Click here to add this to my saved trials
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
Hershey, PA
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated: 1/19/2018
Penn State Milton S. Hershey Medical Center
mi
from
Hershey, PA
Click here to add this to my saved trials
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
Nashville, TN
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated: 1/19/2018
Monroe Carell Jr. Children's Hospital at Vanderbilt
mi
from
Nashville, TN
Click here to add this to my saved trials
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
Dallas, TX
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated: 1/19/2018
University of Texas Southwestern Medical Center
mi
from
Dallas, TX
Click here to add this to my saved trials
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
Houston, TX
Safety and Pharmacokinetic Study of Oral Morphine Sulfate in Pediatric Subjects
A Multicenter, Open Label, Safety and Pharmacokinetic Study of Oral Morphine Sulfate Administration in Pediatric Subjects 2 Years Old Through 17 Years Old With Postoperative Pain
Status: Enrolling
Updated: 1/19/2018
University of Texas Health Science Center at Houston
mi
from
Houston, TX
Click here to add this to my saved trials
Fentanyl Sublingual Spray for the Treatment of Moderate to Severe Post-Operative Pain
A Phase 2 Multicenter, Randomized, Double-Blind, Multiple-Dose, Parallel-Group, Placebo-Controlled Study of Fentanyl Sublingual Spray for the Treatment of Moderate to Severe Post-Operative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
Phoenix, AZ
Fentanyl Sublingual Spray for the Treatment of Moderate to Severe Post-Operative Pain
A Phase 2 Multicenter, Randomized, Double-Blind, Multiple-Dose, Parallel-Group, Placebo-Controlled Study of Fentanyl Sublingual Spray for the Treatment of Moderate to Severe Post-Operative Pain
Status: Enrolling
Updated: 1/19/2018
Arizona Research Center
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Fentanyl Sublingual Spray for the Treatment of Moderate to Severe Post-Operative Pain
A Phase 2 Multicenter, Randomized, Double-Blind, Multiple-Dose, Parallel-Group, Placebo-Controlled Study of Fentanyl Sublingual Spray for the Treatment of Moderate to Severe Post-Operative Pain
Status: Enrolling
Updated:  1/19/2018
mi
from
Anaheim, CA
Fentanyl Sublingual Spray for the Treatment of Moderate to Severe Post-Operative Pain
A Phase 2 Multicenter, Randomized, Double-Blind, Multiple-Dose, Parallel-Group, Placebo-Controlled Study of Fentanyl Sublingual Spray for the Treatment of Moderate to Severe Post-Operative Pain
Status: Enrolling
Updated: 1/19/2018
Anaheim Clinical Trials, LLC
mi
from
Anaheim, CA
Click here to add this to my saved trials
Comparative Bioavailability Study of Morphine Sulfate Immediate Release and Controlled Release
A Single Dose, Three-Period, Three-Treatment, Six-Sequence, Three-Way Crossover Comparative Bioavailability Study of Morphine Sulfate Immediate Release Tablets and Solution and Controlled Release Capsules Under Steady-State Conditions.
Status: Enrolling
Updated:  1/19/2018
mi
from
Austin, TX
Comparative Bioavailability Study of Morphine Sulfate Immediate Release and Controlled Release
A Single Dose, Three-Period, Three-Treatment, Six-Sequence, Three-Way Crossover Comparative Bioavailability Study of Morphine Sulfate Immediate Release Tablets and Solution and Controlled Release Capsules Under Steady-State Conditions.
Status: Enrolling
Updated: 1/19/2018
CEDRA Clinical Research, LLC
mi
from
Austin, TX
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Dose Proportionality and Food Effect of Morphine Sulfate
A Single Dose, Three-Period, Three-Treatment, Six-Sequence, Three-Way Crossover Study of the Dose Proportionality of and Effect of Food on Morphine Sulfate Tablets.
Status: Enrolling
Updated:  1/19/2018
mi
from
Austin, TX
Dose Proportionality and Food Effect of Morphine Sulfate
A Single Dose, Three-Period, Three-Treatment, Six-Sequence, Three-Way Crossover Study of the Dose Proportionality of and Effect of Food on Morphine Sulfate Tablets.
Status: Enrolling
Updated: 1/19/2018
CEDRA Clinical Research, LLC
mi
from
Austin, TX
Click here to add this to my saved trials
Bioequivalency Study of Morphine Sulfate Injection, Solution and Tablet Under Fasted Conditions
A Single Dose, Three-Period, Three-Treatment, Six-Sequence, Three-Way Crossover Pharmacokinetic and Comparative Bioavailability Study of Morphine Sulfate Injection, Solution, and Tablet Formulations Under Fasting Conditions.
Status: Enrolling
Updated:  1/19/2018
mi
from
Austin, TX
Bioequivalency Study of Morphine Sulfate Injection, Solution and Tablet Under Fasted Conditions
A Single Dose, Three-Period, Three-Treatment, Six-Sequence, Three-Way Crossover Pharmacokinetic and Comparative Bioavailability Study of Morphine Sulfate Injection, Solution, and Tablet Formulations Under Fasting Conditions.
Status: Enrolling
Updated: 1/19/2018
CEDRA Clinical Research, LLC
mi
from
Austin, TX
Click here to add this to my saved trials
Dose Linearity Study of Codeine Sulfate Under Fasted Conditions
A Single Dose, 3-Period, 3-Treatment, 6-Sequence, 3-Way Crossover Study of the Dose Linearity of Codeine Sulfate Tablets Under Fasting Conditions
Status: Enrolling
Updated:  1/19/2018
mi
from
Austin, TX
Dose Linearity Study of Codeine Sulfate Under Fasted Conditions
A Single Dose, 3-Period, 3-Treatment, 6-Sequence, 3-Way Crossover Study of the Dose Linearity of Codeine Sulfate Tablets Under Fasting Conditions
Status: Enrolling
Updated: 1/19/2018
CEDRA Clinical Research, LLC
mi
from
Austin, TX
Click here to add this to my saved trials
Steady State Study of Codeine Sulfate
A Single Dose, 1-Period, 1-Treatment Study of Codeine Sulfate 15 mg Tablets Under Steady State Conditions
Status: Enrolling
Updated:  1/19/2018
mi
from
Austin, TX
Steady State Study of Codeine Sulfate
A Single Dose, 1-Period, 1-Treatment Study of Codeine Sulfate 15 mg Tablets Under Steady State Conditions
Status: Enrolling
Updated: 1/19/2018
CEDRA Clinical Research, LLC
mi
from
Austin, TX
Click here to add this to my saved trials
Food Effect Study of Codeine Sulfate
A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Codeine Sulfate Tablets Under Fasting and Fed Conditions
Status: Enrolling
Updated:  1/19/2018
mi
from
San Antonio, TX
Food Effect Study of Codeine Sulfate
A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Codeine Sulfate Tablets Under Fasting and Fed Conditions
Status: Enrolling
Updated: 1/19/2018
CEDRA Clinical Research, LLC
mi
from
San Antonio, TX
Click here to add this to my saved trials
Pharmacokinetic and Comparative Bioavailability Study of Codeine Sulfate Under Fasted Conditions
A Single Dose, 3-Period, 3-Treatment, 6-Sequence Crossover Pharmacokinetic and Comparative Bioavailability Study of Codeine Sulfate Tablet Formulations Under Fasting Conditions
Status: Enrolling
Updated:  1/19/2018
mi
from
San Antonio, TX
Pharmacokinetic and Comparative Bioavailability Study of Codeine Sulfate Under Fasted Conditions
A Single Dose, 3-Period, 3-Treatment, 6-Sequence Crossover Pharmacokinetic and Comparative Bioavailability Study of Codeine Sulfate Tablet Formulations Under Fasting Conditions
Status: Enrolling
Updated: 1/19/2018
CEDRA Clinical Research, LLC
mi
from
San Antonio, TX
Click here to add this to my saved trials
Comparative Bioavailability Study of Codeine Sulfate
A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Comparative Bioavailability Study fo Codeine 30 mg Tablets and Tylenol #3 Tablets Under Fasting Conditions
Status: Enrolling
Updated:  1/19/2018
mi
from
San Antonio, TX
Comparative Bioavailability Study of Codeine Sulfate
A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Comparative Bioavailability Study fo Codeine 30 mg Tablets and Tylenol #3 Tablets Under Fasting Conditions
Status: Enrolling
Updated: 1/19/2018
CEDRA Clinical Research, LLC
mi
from
San Antonio, TX
Click here to add this to my saved trials
Bioequivalency Study of Oxymorphone Hydrochloride 10 mg Tablets Under Fasted Conditions
A Single Dose, Two-Period, Two-Treatment, Two-Sequence Crossover Bioequivalence Study of Oxymorphone Hydrochloride IR 10 mg Tablets, With a Naltrexone Block, Under Fasted Conditions
Status: Enrolling
Updated:  1/19/2018
mi
from
Houston, TX
Bioequivalency Study of Oxymorphone Hydrochloride 10 mg Tablets Under Fasted Conditions
A Single Dose, Two-Period, Two-Treatment, Two-Sequence Crossover Bioequivalence Study of Oxymorphone Hydrochloride IR 10 mg Tablets, With a Naltrexone Block, Under Fasted Conditions
Status: Enrolling
Updated: 1/19/2018
Novum Pharmaceutical Research Services
mi
from
Houston, TX
Click here to add this to my saved trials
The Effect of Neurontin on Pain Management in the Acutely Burned Patient
The Effect of Neurontin on Pain Management in the Acutely Burned Patient
Status: Enrolling
Updated:  1/22/2018
mi
from
Iowa City, IA
The Effect of Neurontin on Pain Management in the Acutely Burned Patient
The Effect of Neurontin on Pain Management in the Acutely Burned Patient
Status: Enrolling
Updated: 1/22/2018
University of Iowa Burn Center
mi
from
Iowa City, IA
Click here to add this to my saved trials
Dexamethasone and Pain Following Total Knee Arthroplasty
Perioperative Dexamethasone to Promote Systemic Pro-Resolution Phenotype for Prevention of Acute and Chronic Pain Post-Total Knee Arthroplasty.
Status: Enrolling
Updated:  1/22/2018
mi
from
Durham, NC
Dexamethasone and Pain Following Total Knee Arthroplasty
Perioperative Dexamethasone to Promote Systemic Pro-Resolution Phenotype for Prevention of Acute and Chronic Pain Post-Total Knee Arthroplasty.
Status: Enrolling
Updated: 1/22/2018
DUMC
mi
from
Durham, NC
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Determination of ED90 of Intrathecal Lidocaine for Adequate Anesthesia for Elective Cervical Cerclage Surgery
Determination of ED90 of Intrathecal Lidocaine for Adequate Anesthesia for Elective Cervical Cerclage Surgery
Status: Enrolling
Updated:  1/22/2018
mi
from
Chicago, IL
Determination of ED90 of Intrathecal Lidocaine for Adequate Anesthesia for Elective Cervical Cerclage Surgery
Determination of ED90 of Intrathecal Lidocaine for Adequate Anesthesia for Elective Cervical Cerclage Surgery
Status: Enrolling
Updated: 1/22/2018
Prentice Women's Hospital
mi
from
Chicago, IL
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Choosing Opioid Management for Pain and Analyzing Acute Chest Syndrome (ACS) Rates Equally
Choosing Opioid Management for Pain and Analyzing ACS Rates Equally
Status: Enrolling
Updated:  1/23/2018
mi
from
Atlanta, GA
Choosing Opioid Management for Pain and Analyzing Acute Chest Syndrome (ACS) Rates Equally
Choosing Opioid Management for Pain and Analyzing ACS Rates Equally
Status: Enrolling
Updated: 1/23/2018
Children's Healthcare of Atlanta
mi
from
Atlanta, GA
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An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated:  1/23/2018
mi
from
Metairie, LA
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated: 1/23/2018
Clinical Research Facility
mi
from
Metairie, LA
Click here to add this to my saved trials
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated:  1/23/2018
mi
from
Jacksonville, FL
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated: 1/23/2018
Clinical Research Facility
mi
from
Jacksonville, FL
Click here to add this to my saved trials
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated:  1/23/2018
mi
from
Prairie Village, KA
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated: 1/23/2018
Clinical Research Facility
mi
from
Prairie Village, KA
Click here to add this to my saved trials
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated:  1/23/2018
mi
from
Mandeville, LA
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated: 1/23/2018
Clinical Research Facility
mi
from
Mandeville, LA
Click here to add this to my saved trials
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated:  1/23/2018
mi
from
New Orleans, LA
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated: 1/23/2018
Clinical Research Facility
mi
from
New Orleans, LA
Click here to add this to my saved trials
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated:  1/23/2018
mi
from
Oklahoma City, OK
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated: 1/23/2018
Clinical Research Facility
mi
from
Oklahoma City, OK
Click here to add this to my saved trials
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated:  1/23/2018
mi
from
Clinton, UT
An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)
An Open-label, Multi-center, Single-arm, Phase IV Clinical Trial Assessing Conversion From Hydrocodone, Oxycodone CR or Morphine SR to Tapentadol ER in Subjects With Moderate to Severe Chronic Low Back or OA Pain of the Hip or Knee
Status: Enrolling
Updated: 1/23/2018
Clinical Research Facility
mi
from
Clinton, UT
Click here to add this to my saved trials
Manual Therapy to Treat Gluteus Medius Trigger Points
Manual Therapy to Treat Gluteus Medius Trigger Points to Improve Hip Abduction Strength in Patients With Anterior Knee Pain.
Status: Enrolling
Updated:  1/23/2018
mi
from
Columbus, OH
Manual Therapy to Treat Gluteus Medius Trigger Points
Manual Therapy to Treat Gluteus Medius Trigger Points to Improve Hip Abduction Strength in Patients With Anterior Knee Pain.
Status: Enrolling
Updated: 1/23/2018
Nationwide Children's Hospital Sports and Ortho PT East Broad
mi
from
Columbus, OH
Click here to add this to my saved trials
Effectiveness of the Precision Spinal Cord Stimulator System at Sub-Perception Amplitude
WHISPER - A Randomized Controlled Study to Evaluate the Effectiveness of the Precision Spinal Cord Stimulator System at Sub-Perception Amplitude
Status: Enrolling
Updated:  1/23/2018
mi
from
Valencia, CA
Effectiveness of the Precision Spinal Cord Stimulator System at Sub-Perception Amplitude
WHISPER - A Randomized Controlled Study to Evaluate the Effectiveness of the Precision Spinal Cord Stimulator System at Sub-Perception Amplitude
Status: Enrolling
Updated: 1/23/2018
Boston Scientific Clinical Research Information Toll Free Number
mi
from
Valencia, CA
Click here to add this to my saved trials
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome: A Randomized Controlled Trial
Status: Enrolling
Updated:  1/23/2018
mi
from
Columbus, OH
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome: A Randomized Controlled Trial
Status: Enrolling
Updated: 1/23/2018
Nationwide Children's Hospital Sports and Ortho PT East Broad
mi
from
Columbus, OH
Click here to add this to my saved trials
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome: A Randomized Controlled Trial
Status: Enrolling
Updated:  1/23/2018
mi
from
Dublin, OH
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome: A Randomized Controlled Trial
Status: Enrolling
Updated: 1/23/2018
Nationwide Children's Hospital Sports and Ortho PT Dublin
mi
from
Dublin, OH
Click here to add this to my saved trials
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome: A Randomized Controlled Trial
Status: Enrolling
Updated:  1/23/2018
mi
from
New Albany, OH
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome: A Randomized Controlled Trial
Status: Enrolling
Updated: 1/23/2018
Nationwide Children's Hospital Sports and Ortho PT New Albany
mi
from
New Albany, OH
Click here to add this to my saved trials
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome: A Randomized Controlled Trial
Status: Enrolling
Updated:  1/23/2018
mi
from
Westerville, OH
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome
Evaluation of a Treatment Algorithm for Patients With Patellofemoral Pain Syndrome: A Randomized Controlled Trial
Status: Enrolling
Updated: 1/23/2018
Nationwide Children's Hospital Sports and Orthopedic PT Westerville location
mi
from
Westerville, OH
Click here to add this to my saved trials