OSA Screen Negative With Spinal Duramorph



Status:Terminated
Conditions:Depression, Depression, Pulmonary
Therapuetic Areas:Psychiatry / Psychology, Pulmonary / Respiratory Diseases
Healthy:No
Age Range:18 - 50
Updated:9/9/2018
Start Date:August 3, 2015
End Date:October 1, 2015

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Trial Summary
Trial Overview
Inclusion Criteria

A Prospective, Observational, Double-blind (Black-Box) Study Evaluating Incidence, Severity and Predictive Factors of Respiratory Depression and Sleep Disorder Pattern During Postoperative Neuraxial Opioid Analgesia in OSA Screened Negative With BMI>=35 Kg/m2 Obstetric Patients After Cesarean Delivery Using Current Standard Intermittent Postoperative Monitoring Compared to Continuous Pulse Oximetry/Capnography

Non emergent scheduled cesarean sections will be consented to participate in this study of
patients who have screened negative for obstructive sleep apnea and who are also BMI>/= 35 to
have capnography monitoring postoperatively. The capnography and pulse oximetry will be
initiated in the post anesthesia care unit and be worn for 12-24 hours after delivery. Data
will be retrieved after that time period in a deidentified fashion. Medication usage will be
reviewed as well as the standard of care information from the duramorph monitoring will be
retrieved.


Inclusion Criteria:

- OSA screen negative per hospital protocol

- age 18 or greater

- BMI>35

- consent to participate to wear capnography and pulse oximetry monitoring devices post
delivery

Exclusion Criteria:

- Spanish speaking only

- under age 18

- contraindication to receiving drugs utilized in delivery anesthetic
We found this trial at
1
site
Novant Health Forsyth Medical Center
Winston-Salem, North Carolina 27103
?
mi
from
Winston-Salem, NC
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