Dapagliflozin for Long COVID Syndrome
Starting soon · Phase 3 · Has a placebo group
Conditions studied: COVID - 19, Long COVID Syndrome, SARS CoV-2
In brief
This is a randomized, placebo-controlled study. Patients with long COVID will be randomized to receive dapagliflozin or placebo for 12 months.
Key facts
- Study ID
- NCT06907251
- Run by
- Ottawa Heart Institute Research Corporation
- People needed
- 192
- Starts
- 2026-09-01
- Expected to finish
- 2029-06-30
- Last updated by the study team
- 2026-07-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 18 years of age or older and willing and able to provide informed consent
- Patients with a history of positive COVID-19 test (polymerase chain reaction or rapid test) or have been diagnosed with COVID-19 by a health care provider.
- New or persistent symptoms at least 12 weeks from infection and present for at least 8 weeks that is not explained by an alternative diagnosis (64).
- Women of childbearing potential (WOCBP) who, if sexually active, are willing to use to use at least one highly effective methods of contraception throughout the study.
You may not qualify if…
- History of diabetes
- Prior heart failure
- Weight loss treatment with glucagon-like peptide-1 receptor agonists (e.g. liraglutide, semaglutide)
- Pregnancy or planned pregnancy in the next 12 months. We will ask WOCBP about the possibility of pregnancy at the time of screening and if so, then pregnancy testing will be offered. If testing is declined in this instance, then they will be excluded from the study.
- Women who are breastfeeding
- Severe renal impairment (eGFR<30mL/min1.73m2)
- Known history of allergy or hypersensitivity to dapagliflozin
- Exclusion for optional MRI portion of the protocol:
- Any contraindication to MRI
Where it is running
- University of Ottawa Heart Institute — Ottawa, Ontario, Canada
Full record on ClinicalTrials.gov
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