Clinical trial Recruiting at 1 site Observational Ages 18 and up

Biomarkers for opioid use and pain response after trauma and surgery

Official title: Identifying Biomarkers Related to Opioid Use and Pain Response Following Traumatic Injury and Surgery

Run by University of California, San Diego · NCT07693270 · Data updated 2026-11-12

This study tests whether microRNA patterns can predict long-term opioid risk in adults after trauma or surgery.

More Opioid Use Disorder trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorUniversity of California, San Diego
Academic / other
Locations1 site (La Jolla, California)
StatusRecruiting
StartedJuly 15, 2026
Main results expectedJune 2027
Study endsJune 2027
Registry record updatedJuly 17, 2026
Trial IDNCT07693270 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years or older admitted for traumatic injury or undergoing specified surgeries (orthopedic, abdominal, breast, vascular, or thoracic) at UC San Diego.

Probably not a fit

Patients with a history of opioid use disorder, pregnant individuals, prisoners, or those unable to consent are less likely to benefit from this biomarker-focused study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study will examine miRNA expression dynamics in patients treated with opioids following traumatic injury or surgical procedures. Researchers will collect behavioral data and genomic information to see if miRNA signatures can better predict persistent opioid use and pain outcomes than current tools. The goal is to develop a scalable screening approach to identify individuals at higher risk for opioid use disorder after prescription opioid use. The work follows Wellcome Leap goals to quantify addiction risk and progression during pain management. No interventions are being tested in this study; the focus is on biomarker discovery and feasibility.

Why it matters

Potential benefit: If successful, the study could lead to a high-throughput test that helps predict who is at risk for long-term opioid problems after injury or surgery.

How similar studies have gone: Prior biomarker and genomic studies suggest miRNA signals can reflect pain and opioid responses, but this approach remains exploratory and feasibility-focused.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients 18 years of age or older
* Patients admitted for traumatic injury at Hillcrest or Jacobs Medical Center or patients who will undergo the orthopedic (e.g., joint, spine), abdominal, breast, vascular (e.g., amputation), or thoracic surgery.

Exclusion Criteria:

* Patients with a prior history of opioid use disorder or dependence
* Pregnant women
* Prisoners
* Patients with an inability to independently provide informed consent to participate in the study due to lack of capacity. This lack of capacity can be from either a chronic/continuous condition (i.e. dementia), or can be temporary (i.e. clear signs of intoxication at the time of the visit (not alert or oriented, slurring words \[and confirmed not to be baseline\], unsteady gait \[and confirmed not to be baseline\], or appears impaired based on clinical judgement by PI/Co-I)).

Where it's running

  • University of California, San Diego
    La Jolla, California, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.