Survey Study for Pain Management, Wound Care, Scar Care or UDT

Pain Clinical Trial

Official title: 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.

Status Recruiting

Clinical Trial Summary

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.

Clinical Trial 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:

• 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. ;

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

• Pain
• Scars
• Urinary Drug Testing
• Wounds

• NCT number: NCT02195063
• Study type: Observational
• Source: Rahm Foundation
• Contact: Christina R Cook, PhD
• Phone: 615-712-9574
• Email: ccook@blueprintpathways.com
• Status: Recruiting
• Phase: Phase 4
• Start date: November 2013