Could a CoQ10 supplement counteract GLP-1 fatigue and muscle loss?
NCT ID NCT07789106
First seen Aug 27, 2026 · Last updated Sep 02, 2026 · Updated 3 times
Summary
This trial tests whether a daily ubiquinol supplement, a form of Coenzyme Q10, can reduce fatigue and help maintain muscle strength in adults aged 30-65 who are taking GLP-1 weight loss medications like Wegovy or Mounjaro. About 90 participants will take either ubiquinol or a placebo capsule every day for 9 months. Researchers will measure fatigue, muscle function, and quality of life through home nurse visits, monthly video calls, and smartphone app logging. The study is fully remote, so participants do not need to visit a clinic.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ubiquinol (a form of Coenzyme Q10) taken as a 100 mg oral capsule daily
- What this could lead to
- If it works, this could point toward a simple daily supplement that helps people on GLP-1 weight loss medications feel less tired and keep more muscle strength.
- What could go wrong
- This is a small, early-stage trial with 90 participants, so results may not apply broadly. The supplement might not outperform the placebo, and any benefit could be modest.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 90 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Sep 2026
An estimate. Start dates often move.
- Expected to finish
-
Sep 2028
An estimate. End dates often move.
- Lead sponsor
-
A research network
The lead sponsor is a research network or cooperative group.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
30 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 30-65 years * Body mass index \>27kg/m2 and \<35 kg/m2 * Currently initiating, or has initiated within the preceding 4 weeks of screening, one of the following MHRA-licensed weight management pharmacotherapies: semaglutide 2.4mg (Wegovy®) or tirzepatide (Mounjaro®) prescribed for the indication of weight management. * Is physically mobile and able to complete 5x sit to stand movements * Owns a smartphone (iOS 15.6 or later, Android 9 or later) and is willing and able to install the SANNO Health app * Proficient in English language speaking and reading * Owns their own digital body weighing scale * Able and willing to provide full informed consent Exclusion Criteria: * Prior use of ubiquinol or Co-enzyme Q10 within 3 months of screening * Diagnosed condition which, in the opinion of the Chief investigator, may independently impact fatigue (e.g. type 1 or type 2 diabetes, cardiovascular disease, obstructive sleep apnoea, inflammatory or autoimmune conditions, cirrhotic or advanced liver disease, malignancy) * Prior or current use of statin medication * Has previously used GLP-1 agonists and/or undergone bariatric surgery * Other medications, which in the opinion of the Chief Investigator, may deplete CoQ10 * Failed screening bloods (any results that is outside of the lab reference range) * Intention to stop GLP-1 agonist use within 9 months of randomisation * Pregnancy, breastfeeding or intention to conceive during study
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Fatigue severity scale are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Office 1110 3 Fitzroy Place, 1/1, Sauchiehall Street
Glasgow, G3 7RH, United Kingdom
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Real-World effectiveness, safety, and Patient-Reported outcomes of tirzepatide in adults with type 2 diabetes mellitus, obesity, or prediabetes in pakistan: a multicentre, prospective, observational cohort study
- Combined inspiratory muscle training and functional High-Intensity interval training promote respiratory, diaphragmatic, and aerobic adaptations in children with obesity
- Relationship between Collagen-Containing supplement use and muscle mass and body image following metabolic and bariatric surgery: a prospective observational study
- Can a dash of spice and protein shield muscle during Weight-Loss shots?
- Could a sirtuin boost make dieting more effective?
- Can a High-Protein or High-Fat Low-Carb diet tame blood sugar and triglycerides?