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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.
Full description
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:
Datum Research will need to have access to the prescription to see what compound was prescribed.
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Inclusion criteria
Exclusion criteria
10,000 participants in 4 patient groups
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Central trial contact
Christina R Cook, PhD; Risa Tyo, PharmD
Data sourced from clinicaltrials.gov
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