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Lexington Observational Study of Treatment With Compounded Pain Creams

NCT02195752 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 26

Last updated 2015-05-12

No results posted yet for this study

Summary

A two-year + 3 Mo. observational study to track compliance and outcomes in adult patients prescribed compounded pharmaceutical creams for the treatment of pain. The project is designed to accumulate tracking information from both patients and physicians over the course of therapy as a supplement to the ordinary care that the patients will normally receive. We seek to discover aspects of successful and unsuccessful treatment using topical pain creams. This information will be analyzed and reports prepared of observations and emergent findings. These reports will be sent during the study every 1 or 2 months to patients, physicians and pharmacists who are participating in the Study. A final compilation of findings and observations will be circulated to participating patients, physicians and pharmacists.

Conditions

Interventions

OTHER

Compounded Pain Cream

All patients will have been prescribed a topical pain cream prepared by a qualified compounding pharmacy

Sponsors & Collaborators

  • Palm Beach CRO

    collaborator UNKNOWN

  • Lexington Independent Studies, LLC

    lead INDUSTRY

Principal Investigators

  • Stephen A. Raymond, PhD · Research and Marketing Consultants

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2015-04-30
Completion
2015-05-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02195752 on ClinicalTrials.gov