Lexington Observational Study of Treatment With Compounded Pain Creams

Stopped early

Conditions studied: Chronic Pain, Acute Pain

In brief

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.

Key facts

Study ID

NCT02195752

Run by

Lexington Independent Studies, LLC

People needed

26

Starts

2014-11-01

Expected to finish

2015-05-01

Last updated by the study team

2015-05-12

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• be informed of the nature of the study and must give written informed consent
• be able to communicate effectively with study personnel
• be diagnosed with a condition for which the physician has prescribed a compounded pain cream.

You may not qualify if…

• History of allergy or adverse reaction to pain cream ingredients
• History of psychiatric disorders

Where it is running

• Lido Chen — Laguna Hills, California, United States
• Adolphus Anekwe — Gary, Indiana, United States

Full record on ClinicalTrials.gov

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