Relieving Pain and Improving Sleep: Evaluating Topical Pain Relief and Sleep Patches

Enrolling by invitation · Not applicable · Has a placebo group

Conditions studied: Pain, Back, Pain, Acute, Sleep Disorder, Sleep Disorders, Circadian Rhythm, Sleep, Sleep Deprivation, Insomnia

In brief

This minimal risk, randomized, double-blind, placebo controlled Institutional Review Board (IRB)-approved study with functional measurements, will evaluate pain relief and sleep improvement after use of a drug- free, non-invasive patch (FREEDOM or REM Patch; The Super Patch Company Inc.); using validated scales and functional measurement tools along with crossover and control groups within the same subject group not receiving an 'active' patch.

Key facts

Study ID

NCT06505005

Run by

SuperPatch Limited LLC

People needed

150

Starts

2024-09-20

Expected to finish

2026-05-01

Last updated by the study team

2025-12-08

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Ages 18-64
• Ability to provide Informed Consent
• Received a study patch (active or sham) from their treating clinician (randomized) for back, shoulder, and other musculoskeletal pain.
• Has been diagnosed with an acute, moderate pain condition
• Agrees to wear an adhesive study patch during the study period

You may not qualify if…

• Patients who are beneficiaries of a government-funded healthcare program
• Use of drugs of abuse (illicit or prescription)
• Have an implanted device, or wears, or adheres any electrical device to the body during the study, other than a hearing aid.

Where it is running

• Stein Medical — Tyrone, Georgia, United States

Full record on ClinicalTrials.gov

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