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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 23 January 2023
Main ID:  NCT02674958
Date of registration: 06/01/2016
Prospective Registration: Yes
Primary sponsor: Ottawa Heart Institute Research Corporation
Public title: Mobilization of Endothelial Progenitor Cells and Aspirin TROPHIC 3
Scientific title: Mobilization of Endothelial Progenitor Cells Following Alcohol Septal Ablation in Hypertrophic Obstructive Cardiomyopathy: Randomized Controlled Trial of Aspirin
Date of first enrolment: May 2016
Target sample size: 6
Recruitment status: Terminated
URL:  https://clinicaltrials.gov/show/NCT02674958
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Basic Science. Masking: Single (Outcomes Assessor).  
Phase:  Phase 3
Countries of recruitment
Canada
Contacts
Name:     Aun-Yeong Chong, MD, MRCP
Address: 
Telephone:
Email:
Affiliation:  OHIRC
Key inclusion & exclusion criteria

Inclusion Criteria:

1. Patients who have been selected to undergo alcohol septal ablation for hypertrophic
obstructive cardiomyopathy based on clinical need

2. Age >18 years, <80 years

Exclusion Criteria:

1. Patients with known allergy to aspirin

2. Inability or refusal to consent to participate in the study

3. Patients who are on non-steroidal anti-inflammatory drugs and cannot be stopped for
the duration of the study



Age minimum: 18 Years
Age maximum: 80 Years
Gender: All
Health Condition(s) or Problem(s) studied
Hypertrophic Obstructive Cardiomyopathy
Intervention(s)
Drug: Aspirin
Primary Outcome(s)
Maximum circulating endothelial progenitor cells as a ratio to baseline at any timepoint [Time Frame: 0 hour, 1 hour, 6 hours, 24 hours, 72 hours and 7 days]
Secondary Outcome(s)
Endothelial cell migration in vitro compared to baseline at any timepoint [Time Frame: 0 hour, 1 hour, 6 hours, 24 hours, 72 hours and 7 days]
Secondary ID(s)
20150432
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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