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Topical Compounded Pain Creams And Pain Perception (TOPCAPP)

M

Medimix Specialty Pharmacy, LLC

Status

Completed

Conditions

Pain

Study type

Observational

Funder types

Industry

Identifiers

NCT01862848
Medimix Pharm-01

Details and patient eligibility

About

To evaluate the change in patient pain perception with the use of a topical compounded pain cream regimen.

Full description

This is a prospective,observational,single center, open label study of patients that receive a combination topical compounded analgesic medication with no comparator group.

Enrollment

285 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants must be diagnosed with an ICD9 code indicative of chronic pain.
  • Participants must be starting a new regimen of topical therapy with multiple compounded agents.
  • Participants must be expecting to receive therapy for at least 12 weeks.
  • Participants must be between 18 and 65 years of age.
  • Participants must be able to provide sound written and verbal informed consent.

Exclusion criteria

  • Participants must not have prior hypersensitivity or adverse events to any of the components in the customized prescription.
  • Participants must not be pregnant or breastfeeding women.
  • Participants must not have a diagnosis of cancer within the past 5 years.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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