An Artificial Intelligence Driven Approach to Optimize Patient Selection for a Transitional Pain Service

Study acronym: TPS-Select
StatusNot Yet Recruiting
PhasePhase 3
Started

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Trial flagged as At Risk
Primary completion moved at least 12 months later Dec 1, 2027 → Dec 1, 2028
Primary endpoint reworded 1 of 1 changed
See other at-risk trials from University of California, San Francisco

Record History

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  1. Primary completion pushed from Dec 1, 2027 to Dec 1, 2028 Show 5 more changesShow less
    • Primary endpoint(s) modified
    • Enrollment increased: 126 → 474 participants
    • Study completion pushed from Jul 1, 2028 to Dec 1, 2029
    • Eligibility criteria expanded, about 19 words
    • Secondary endpoints: 3 to 4
  2. Start date: May 1, 2026 to Oct 1, 2026v2
  3. Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
The goal of this clinical trial is to learn whether a pain-management program called a Transitional Pain Service can help prevent long-term pain and reduce opioid needs after surgery in adult surgical patients who may be at higher risk for developing persistent pain. The main questions this trial aims to answer are: 1) Does the Transitional Pain Service help high-risk surgical patients manage pain better after surgery? 2) Can a computer tool (an algorithm) improve screening of patients for long-lasting pain after surgery? The investigators will compare patients who continue with their usual care to patients who receive support from the Transitional Pain Service to see if the program leads to better pain control and lower opioid use. Participants will share information about their pain levels and the pain-relief treatments they are using before and after surgery so researchers can better understand how the program affects recovery. Patients assigned to the Transitional Pain Service will also be offered additional coordinated support before and after their surgery to help optimize their pain control and overall recovery.
Trial Details
NCT Number NCT07296770
Lead Sponsor University of California, San Francisco
Conditions
(from sponsor)		 Postsurgical Pain Management, Postsurgical Pain, Chronic, Opioid Use After Surgery
Related terms Pain, Postoperative Pain
Enrollment 474 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov