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Effect of Colchicine on the Progression of Aortic Valve Stenosis - a Pilot Study

Effect of Colchicine on the Progression of Aortic Valve Stenosis - a Pilot Study

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05253794
Acronym
COPAS-Pilot
Enrollment
24
Registered
2022-02-24
Start date
2022-07-01
Completion date
2026-09-30
Last updated
2024-12-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Stenosis, Inflammation

Keywords

colchicine

Brief summary

COPAS pilot is a pilot single center double blinded randomized study to determine the effect of targeted anti-inflammation therapy using colchicine, on valvular calcification activity using imaging, i.e. aortic valvular NaF uptake. The current proposal uses a randomized design to evaluate the effect of colchicine vs. placebo on valvular calcification activity over 6 months measured using NaF PET

Detailed description

COPAS pilot is a pilot single center double blinded randomized study. The investigators will compare the effect of colchicine (0.6 mg daily - intervention arm) vs. placebo (control group) on the 18F NaF aortic valve uptake in patients with mild to moderate AS defined by a mean pressure gradient measured using transthoracic echocardiography (TTE) between 15-25 mm Hg after a 6-month period of treatment. The investigators plan to enroll 12 patients (6 males/6 females) in each arm (total sample size: 24 patients). Primary endpoint is the change in 18FNaF aortic valve uptake between baseline and 6 months in each arm. Parameters of interest are the maximal and total standard uptake values (SUVs) and tissue-to background ratios (TBRs) at the level of the aortic valve.

Interventions

oral tablet daily for 6 months

DRUGPlacebo

oral tablet daily for 6 months

Sponsors

Ottawa Heart Institute Research Corporation
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. mild to moderate aortic stenosis defined by a mean pressure gradient using transthoracic echocardiography (TTE) between 15-25mmHg. 2. age greater than18 years; 3. given informed consent.

Exclusion criteria

1. bicuspid aortic valve 2. associated moderate to severe aortic regurgitation 3. associated other valvular pathology of moderate or greater severity 4. LV dysfunction (EF\<50%); 5. decompensated heart failure; 6. active infection (e.g. pneumonia, active skin infections, and on antibiotics); 7. chronic diarrhea; 8. immune compromise (e.g. recurrent infection); 9. history of cancer within the last 3 years (other than a successfully treated cutaneous squamous cell or basal cell carcinoma or localized carcinoma in situ of the cervix). 10. active inflammatory conditions (e.g. rheumatoid arthritis, chronic inflammatory bowel disease, SLE, systemic anti-inflammatory therapy (e.g. prednisone, methotrexate)); 11. pregnancy (all women of child bearing potential will have a negative BHCG test; 12. breastfeeding; 13. 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. 14. glomerular filtration rate (GFR) \<50 ml/min/1.72m2; 15. Use of p-glycoprotein inhibitor (e.g. cyclosporine, verapamil, or quinidine) or a strong CYP3A4 inhibitor (e.g. ritonavir, clarithromycin, or ketoconazole); 16. Hemoglobin \< 105(women) \<110 (men) g/L; WBC \< 3.0x 10(9)/L, platelet count\< 110x 10(9)/L; 17. 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. 18. unable to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
Change in aortic valve calcification activity6 monthsChange in valvular calcification activity as measured by NaF uptake by Target to Background Ratio (TBR) on PET/CT imaging

Other

MeasureTime frameDescription
Change in aortic valve calcificationOne yearChange is the degree of aortic valve calcification measured using CT scan (calcium score) and expressed in arbitrary units

Countries

Canada

Contacts

Primary ContactDavid Messika-Zeitoun
DMessika-zeitoun@ottawaheart.ca613 796 7000
Backup ContactKevin E Boczar
kboczar@ottawaheart.ca613 796 7000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026