CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 70 enrolled
Drug / intervention
Icosapent Ethyl 1000 MG Oral Capsule [Vascepa]drug
Likely dose
Icosapent Ethyl 1000 MG Oral Capsule [Vascepa]from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04562467
NCT04562467Phase 4Completed

The Icosapent Ethyl and Prevention of Vascular Regenerative Cell Exhaustion Study

Canadian Medical and Surgical Knowledge Translation Research Group·interventional·Posted Sep 24, 2020·Updated Apr 2, 2024

In Brief

A Phase 4 clinical trial evaluating Icosapent Ethyl 1000 MG Oral Capsule [Vascepa] for Cardiovascular Diseases and 3 related conditions. Completed, enrolled 70 participants across 3 sites.

Detailed Summary

IPE-PREVENTION is a prospective, randomized, 3-month long, open-label study. A total of 70 individuals with elevated cardio-metabolic risk and heightened triglyceride levels, and who are on stable statin therapy will be randomized (1:1) to receive either icosapent ethyl (IPE) 2g BID or standard of care. It is hypothesized that assignment to IPE will lower progenitor cell depletion as well as limit progenitor cell dysfunction. This study may offer some molecular and cellular insights into the mechanisms underlying the cardiovascular benefits of IPE therapy reported in the REDUCE-IT trial.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada

Timeline

Phase 4CompletedFinished
202120222023202420252026
First PostedSep 24, 2020
Enrollment StartSep 24, 2020
Primary CompletionMay 25, 2023
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 5.8 years ago

Interventions

Icosapent Ethyl 1000 MG Oral Capsule [Vascepa]drug

2 x 1g capsules BID as per REDUCE-IT