Taurine Supplementation in Long COVID
- Sponsor
- University of Alberta
- Study ID
- NCT06721949
- Phase
- PHASE2/PHASE3
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Taurine — DRUGTaurine is a naturally occurring amino sulfonic acid commonly found in the body. It is marketed as a natural health product/supplement and plays an important role in the body.
- Placebo — DRUGThe placebo capsule is visually identical to the taurine capsule.
Study Details
The COVID-19 pandemic has swept across the globe, affecting millions of individuals with varying degrees of severity. While many individuals recover from the acute phase of the infection, a significant proportion continue to experience persistent and debilitating symptoms long after the initial SARS-CoV-2 infection. This condition, known as Long COVID (LC) or sometimes referred to as Post-COVID Condition (PCC) or post-acute sequelae of COVID-19, has emerged as a complex multisystemic condition and challenging health issue, affecting approximately 10% of COVID-19 patients. Various symptoms characterize LC, including fatigue, sleep disturbances, cognitive impairment, and mood disturbances. Some of the symptoms are shared with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) - a condition marked by debilitating fatigue and a host of other symptoms without precise biomarkers or objective tests for diagnosis. Effective LC treatments remain elusive and LC patients continue to grapple with persistent symptoms that significantly impact their quality of life. Given the lack of effective treatments, it is imperative to explore novel therapeutic approaches that may alleviate the suffering of this patient population.
Key Dates
- First listed
- Dec 6, 2024
- Start date
- Nov 18, 2025
- Status verified
- May 2026
- Primary completion
- Feb 29, 2028
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 300 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: TaurineParticipants randomized to the Taurine arm will receive two 675 mg taurine capsules twice daily for 12 weeks.
- Placebo Comparator: PlaceboParticipants randomized to the Placebo arm will receive two placebo capsules twice daily for 12 weeks. The placebo capsules will be visually identical to the taurine capsules.
Primary Outcome Measure
Mean change in Modified Fatigue Impact Scale (MFIS) from baseline to three months [ Time Frame: Three months ]
Central Contacts
- Lawrence Richer, MD, MSc780-492-0943
- Ellen Morrison, PhD
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