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NCT06104280: MOUD

Medications for Opioid Use Disorder Photosensitive Retinal Ganglion Cell Function, Sleep, and Circadian Rhythms: Implications for Treatment

Recruiting now Last updated 9 April 2026
What this trial tests

trial testing Post-Illumination Pupillary Response (PIPR) in Opioid Use Disorder in 200 participants. Currently enrolling.

Timeline
6 January 2025
Primary endpoint
28 December 2028
1 January 2029

Quick facts

Lead sponsorUniversity of Alabama at Birmingham
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment200
Start date6 January 2025
Primary completion28 December 2028
Estimated completion1 January 2029
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Alabama at Birmingham

Who can join

Adults 18 to 80, any sex, with Opioid Use Disorder or Sleep Disturbance. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Opioid use disorder (OUD) is a treatable medical illness with three medications FDA approved for treatment. However, persons with OUD report significant sleep disturbance, even when treated with medications for opioid use disorder, leading to high rates of relapse. In this project, we will investigate a special set of photosensitive neurons in the retina as an underlying mechanism for circadian rhythm and sleep disturbance from opioid use and medications for OUD that could lead to novel intervention and improve treatment outcomes.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Opioid Use Disorder

Currently open trials in the same condition.

Other University of Alabama at Birmingham trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06104280.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing