Subjective Observational Study of Patients Using Transdermal Cream Medication And/Or Transdermal Patches With Or Without Oral Non-Narcotic Medications

Data Collection Analysis Business Management

Status: Unknown

Conditions: Pain, Joint; Pain Syndrome; Pain, Chronic

Treatments: Combination Product: transdermal cream and or patch

Study type: Observational

Funder types: Other

Identifiers

NCT03768011

PAS1466

Details and patient eligibility

About

purpose of this study is to evaluate the level of pain perceived by patients using a transdermal cream and/or transdermal patch with or without an oral medication as a pain management solution.

Full description

The purpose of this minimal risk, observational study is to observe and document patients' perspective on how the combination of transdermal cream and/or transdermal patch(s) with or without oral medication can help reduce or eliminate the use of opiate(s).

Enrollment: 5,000 estimated patients

Sex: All

Ages: 18 to 64 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Participants must be diagnosed with an ICD10 code indicative of chronic pain
• Participants must be starting a new regimen of topical therapy with or without non-narcotic oral medication that has been deemed medically necessary and is independent of the study
• Participants must be expecting to receive therapy for at least 12 weeks
• Participants must be between 18 and 64 years of age
• Participants must be able to provide sound verbal informed consent

Exclusion criteria

• Participants must not be a beneficiary of government funded healthcare program (i.e. Medicare, Medicaid, etc.)
• Participants must not have a diagnosis of cancer within the past 5 years
• Participants who have chronic pain conditions not expected to respond to topical pain medication such as deep abdominal pain, or from conditions such as cancer