Survey Study for Pain Management, Wound Care, Scar Care or UDT
| Status: | Recruiting |
|---|---|
| Conditions: | Chronic Pain, Cosmetic |
| Therapuetic Areas: | Dermatology / Plastic Surgery, Musculoskeletal |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/2/2016 |
| Start Date: | November 2013 |
| Contact: | Christina R Cook, PhD |
| Email: | ccook@blueprintpathways.com |
| Phone: | 615-712-9574 |
Survey of Patients Who Have Been Prescribed a Topical Compound for Pain Management, Wound Care or Scar Care or to Patients Who Have Been Requested to do a Urinary Drug Test (UDT) by Their Provider.
This is a survey study that will be given to patients who have been prescribed a topical
compound for pain management, wound care or scar care or to patients who have been requested
to do a urinary drug test (UDT) by their provider.
The initial survey for pain management, wound care, scar care or UDT will be given to the
patient by their providers during their office visit.
compound for pain management, wound care or scar care or to patients who have been requested
to do a urinary drug test (UDT) by their provider.
The initial survey for pain management, wound care, scar care or UDT will be given to the
patient by their providers during their office visit.
We have designed a survey study that will be given to patients who have been prescribed a
topical compound for pain management, wound care or scar care or to patients who have been
requested to do a urinary drug test (UDT) by their provider.
The initial survey for pain management, wound care, scar care or UDT will be given to the
patient by their providers during their office visit.
Follow-up surveys will be given at 30, 60, and 90 days. These surveys will be collected by
e-mail or follow-up calls from Datum Research, LLC, contract research organization.
Data collection for this study will be derived through the 4 patient surveys (initial, 30
day, 60 day, and 90 day) and the prescription written by the provider.
The survey study will enroll patients until December 31, 2014, or until sufficient numbers
have been achieved.
Rahm Foundation will continue the study until:
- Sufficient information has accumulated to meet the scientific objectives of the Study
(i.e. numeric targets or effect size)
- The feasibility of collecting sufficient information diminishes to unacceptable levels,
poor enrollment, loss to follow-up and/or
- Other methods of gathering appropriate information become achievable or are deemed
preferable.
Datum Research will need to have access to the prescription to see what compound was
prescribed.
topical compound for pain management, wound care or scar care or to patients who have been
requested to do a urinary drug test (UDT) by their provider.
The initial survey for pain management, wound care, scar care or UDT will be given to the
patient by their providers during their office visit.
Follow-up surveys will be given at 30, 60, and 90 days. These surveys will be collected by
e-mail or follow-up calls from Datum Research, LLC, contract research organization.
Data collection for this study will be derived through the 4 patient surveys (initial, 30
day, 60 day, and 90 day) and the prescription written by the provider.
The survey study will enroll patients until December 31, 2014, or until sufficient numbers
have been achieved.
Rahm Foundation will continue the study until:
- Sufficient information has accumulated to meet the scientific objectives of the Study
(i.e. numeric targets or effect size)
- The feasibility of collecting sufficient information diminishes to unacceptable levels,
poor enrollment, loss to follow-up and/or
- Other methods of gathering appropriate information become achievable or are deemed
preferable.
Datum Research will need to have access to the prescription to see what compound was
prescribed.
Inclusion Criteria:
- Prescribed a topical cream for pain, scar care, or wound OR Provider preforms urinary
drug test
Exclusion Criteria:
- Subjects with legally authorized representatives
- Minors
- Prisoners
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