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

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).

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