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Study identifier: NCT07135323 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

AvertD Post-Approval Study

Condition: Opioid Use Disorder  ·  Sponsor: Prescient Medicine Holdings, Inc.

PhaseN/A
Planned participants4000
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

A Prospective Post-Approval Study of AvertD to Evaluate Device Performance, Prescribing Impact, and Labeling Comprehension in the Intended Use Population

This description comes directly from the study's public registry record.

Talk to the study team

Amanda Smith, MD  ·  800-800-5525  ·  amanda.smith@concentricsresearch.com

Always discuss trial participation with your own doctor first.

Locations (1)

Concentrics ResearchIndianapolis, Indiana, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07135323