Clareo Health | Subjective Observational Study of Patients Using Transdermal Cream Medication And/Or Transdermal Patches With Or Without Oral Non-Narcotic Medications
Saves the questions and what to expect into your notes, next to the visit they belong to.
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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).
Age
18–64
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
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
You may not be if
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
