Clinical trial Recruiting at 1 site Observational Ages 18 and up

Understanding how duloxetine works for fibromyalgia

Official title: Duloxetine Metabolism and Fibromyalgia

Run by University of Utah · NCT06866444 · Data updated 2026-11-12

This study is trying to see how genetic differences affect how well duloxetine works for people with fibromyalgia, so doctors can better tailor treatments for each patient.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorUniversity of Utah
Academic / other
Locations1 site (Salt Lake City, Utah)
StatusRecruiting
StartedMay 1, 2025
Main results expectedMay 1, 2027
Study endsMay 1, 2027
Registry record updatedSeptember 25, 2026
Trial IDNCT06866444 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18 and older who have been diagnosed with fibromyalgia and are currently taking duloxetine at a dosage of 60 mg/day for at least 8 weeks.

Probably not a fit

Patients who may not benefit from this study include those with progressive illnesses other than fibromyalgia that involve chronic pain and fatigue, as well as individuals with kidney or liver dysfunction.

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 aims to investigate the variability in response to duloxetine treatment among patients with fibromyalgia. It focuses on the relationship between genetic factors that influence drug metabolism and the effectiveness of duloxetine in alleviating symptoms. By analyzing blood concentrations of duloxetine and the genetic variants of drug-metabolizing enzymes, the study seeks to identify which patients are likely to benefit from this medication. The findings could lead to more personalized treatment plans for fibromyalgia patients.

Why it matters

Potential benefit: If successful, this study could help identify which patients are most likely to benefit from duloxetine, leading to more effective and personalized treatment strategies for fibromyalgia.

How similar studies have gone: While there have been studies exploring the pharmacogenomics of duloxetine, this specific approach focusing on fibromyalgia treatment response variability is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults 18+
* Meeting diagnostic criteria for Fibromyalgia
* Patients taking Duloxetine 60 mg/day for at least 8 weeks

Exclusion Criteria:

* Pregnant patients per verbal confirmation
* Patients that have a history of physician diagnosed kidney or liver disfunction or history of renal dialysis.
* Patients requiring an interpreter to communicate
* Patient's with progressive illnesses other than fibromyalgia that have a chronic pain and fatigue component (e.g., cancer patients receiving antineoplastic treatment, Parkinson's disease, Multiple Sclerosis).

Where it's running

  • Pain Management Center and Pain Research Center at the University of Utah
    Salt Lake City, Utah, 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.