Compounded Pain Creams and Patient Perception

Withdrawn before enrolling

Conditions studied: Neurologic Pain, Nociceptive Pain

In brief

There has been a significant increase in the number of prescriptions being filled for Custom Compounded Pain Creams. This study serves to evaluate the patient perception and satisfaction with this type of pain therapy allowing us to identify any statistically relevant relationships that may exist between this type of therapy and patient pain perception. A secondary goal would be to identify any significantly relevant relationships that may exist between this change in pain perception (if any) and the patients overall sense of well-being. The investigators' null hypothesis is that greater that 85% of people will see an significant decrease in perceived pain levels and greater than 85% increase in patient overall sense of well being.

Key facts

Study ID

NCT02024802

Run by

Marwood LowCost Pharmacy

People needed

0

Starts

2014-01-01

Expected to finish

2015-01-01

Last updated by the study team

2014-07-08

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants must be in the range of 18 to 85 years of age as confirmed by state identification or passport presented upon completion of the informed consent.
• Participants must have a diagnosis indicative of either Neuropathic or Nociceptive Pain as confirmed with the prescribing medical provider.
• Participants must be starting a new regimen of transdermal (topic) pain therapy with multiple compounded reagents as indicated on prescription from medical provider
• Participants must be willing to participate in the study for a minimum of 12 weeks
• Participants must be able to provide written informed consent.
• Participants must be able to read and understand the english language

You may not qualify if…

• Participants must not have prior hypersensitivity or adverse events to any components of the customized prescription as indicated by their allergy history given upon registration at the pharmacy.
• Participants must not be pregnant or planning to become pregnant within the 12 week study period and must not be breastfeeding.
• Participants must not have a diagnosis for cancer in the last 5 years.
• Participants legally authorized representative (LAR) will not be a substitute for the participants' written informed consent.

Where it is running

• Marwood Low Cost Pharmacy — Indianapolis, Indiana, United States

Full record on ClinicalTrials.gov

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