A study testing whether a GLP-1 medicine, semaglutide, can help people with spinal cord injuries lower blood sugar.

Recruiting now. Registry record last updated April 13, 2026.

Who can join
Adults 18 to 70, have spinal cord injuries, BMI 22+.
What you take
Semaglutide, given as part of the study. Check ClinicalTrials.gov for this trial's study groups, including any placebo or comparison medicine.
How long it lasts
The full study runs about 4 years.
What you get
Costs vary by study. Ask the study team what this one covers, including the study medicine, visits and travel, before you sign the consent form.
This one may not fit you. We check your age, where you live, and the rules each study sets, then show the clinical trials that do.
Check my fit →
Phase Phase 4Sponsor Marzieh SalehiDrug semaglutideClass GLP-1 RASites 2 USEnrollment target 50

What this study is for

Primary condition: Spinal Cord Injuries. Also studied in: Type 2 Diabetes.

Full scientific study title: Glycemic and Weight Loss Effects of GLP-1R Agonist Therapy in Subjects With Spinal Cord Injury and Type 2 Diabetes.

Who can join

Age18 to 70SexAnyBMI22 or higher

Adults 18 to 70, have spinal cord injuries, BMI 22+. A site coordinator confirms whether you qualify during a free screening visit. The exact medical requirements are below.

Full medical eligibility (for you and your doctor)verbatim from the registry

This is the exact wording from ClinicalTrials.gov, including clinical measures (lab values, imaging scores). Bring it to your doctor if any of it is unclear.

Key inclusion criteria

  • Male and female subjects aged 18-70 years (inclusive) at screening
  • More than one year after spinal cord injury
  • Levels if injury C2-L2 with Asia Impairment Scale A, B, C or D.
  • Provision of signed and dated written informed consent prior to any study specific procedures
  • Diagnosed with T2DM with glucose control managed with diet and metformin monotherapy where no significant dose changes (increase or decrease ≥ 50%) have occurred in the three months prior to screening

Key exclusion criteria

  • History of, or any existing condition that, in the opinion of the investigator, would interfere with evaluation of the investigational product, put the subject at risk, influence the subject's ability to participate or affect the interpretation of the results of the study and/or any subject unable or unwilling to follow study procedures.
  • Any subject who has received another investigational product as part of a clinical study within the last 30 days or 5 half-lives of the drug (whichever is longer) at the time of screening
  • Taking mirabegron or other glucose altering medications
  • Taking steroids within the past 1 year
  • Significant anemia (hemoglobin\<11g/dL)

Where this trial is enrolling

This trial has 2 sites across 1 state. Contact a site coordinator directly to start screening.

Texas2 sites
  • University Health - Texas Diabetic Institute
    San Antonio, Texas
    Matthew A Davisdavism13@uthscsa.edu
  • University of Texas Health Science Center at San Antonio
    San Antonio, Texas
    Matthew A Davisdavism13@uthscsa.edu

Timeline

Started enrolling: April 11, 2025. Expected completion: March 1, 2029. Last updated on ClinicalTrials.gov: April 13, 2026.

Official source

Every Monday we check this trial against ClinicalTrials.gov, the federal registry for clinical research. Last checked September 4, 2026. Confirm the current status there before you contact a site:

View on ClinicalTrials.gov →

Back to the full directory → or take the matching quiz if you want clinical trials filtered to your conditions and location.

Why you can trust GLP Chart. Same scoring framework applied to every program. No paid placements. We never remove unfavorable information at an advertiser's request. Pricing is pulled from each program's public-facing page every Monday.