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NCT05427084RecruitingPhase 2/3

Canagliflozin Targeting Vascular Inflammation

Canagliflozin Targeting Vascular Inflammation: An Ottawa Imaging Study - A Pilot Study

Source: ClinicalTrials.gov · Last updated 6 May 2026

Brief summary (registry, in English)

CANTOR SING is a pilot single center double blinded randomized study. The investigators will compare the effect of canagliflozin (300 mg daily - intervention arm) vs. placebo (control group) on the FDG aortic uptake in patients with stable CAD (over 60 days post-myocardial infarction) after a 6-month period of treatment. The investigators plan to enroll 8 patients in each arm (total sample size: 16 patients). Primary endpoint is the change in FDG aortic uptake between baseline and 6 months in each arm.

Status (registry)
Recruiting
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
24 (estimated)
First submitted
1 Jun 2022
Start date
15 Nov 2024
Primary completion date
Dec 2026
Lead sponsor
Ottawa Heart Institute Research Corporation
NCT number
NCT05427084

What you commit to

  • Study type: Interventional · Phase 2/3
  • Planned participants: 24
  • From 15 Nov 2024 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of p-glycoprotein inhibitor (e.g. cyclosporine, verapamil, or quinidine) or a strong CYP3A4 inhibitor (e.g. ritonavir, clarithromycin, or ketoconazole);

Other illness

  • decompensated heart failure;
  • active infection (e.g. pneumonia, active skin infections, and on antibiotics);
  • active inflammatory conditions (e.g. rheumatoid arthritis, chronic inflammatory bowel disease, SLE, systemic anti-inflammatory therapy (e.g. prednisone, methotrexate));

Lab values

  • glomerular filtration rate (GFR) \<50 ml/min/1.72m2;
  • Hemoglobin \< 105(women) \<110 (men) g/L; WBC \< 3.0x 10(9)/L, platelet count\< 110x 10(9)/L;
  • Patient with a history of cirrhosis, chronic active hepatitis or severe hepatic disease or with alanine aminotransferase (ALT) levels greater than 3 times the upper limit of normal.

Other

  • severe LV dysfunction (EF\<50%);
  • pregnancy (all women of child bearing potential will have a negative BHCG test;
  • breastfeeding;
  • Women of childbearing potential who refuse to use two forms of contraception (this includes at least one form of highly effective and one effective method of contraception) throughout the study OR men capable of fathering a child who refuse to use contraception.
  • unable to give informed consent;

Who the study is looking for

  • 1\) Stable CAD (over 60 days post-myocardial infarction).
  • 2\) Diabetes
  • 3\) given informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University of Ottawa Heart Institute
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OttawaCanadaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.