CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 13 enrolled
Drug / intervention
enalapril maleate +1 moredrug
Likely dose
Not stated in 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/NCT00003070
NCT00003070Phase 3Completed

Afterload Reduction Therapy for Late Anthracycline Cardiotoxicity: A Pediatric Oncology Group Cancer Control Study

Children's Oncology Group·interventional·Posted Mar 1, 2004·Updated Aug 5, 2014

In Brief

A Phase 3 clinical trial evaluating enalapril maleate and quality-of-life assessment for Cardiac Toxicity and Unspecified Childhood Solid Tumor, Protocol Specific. Completed, enrolled 13 participants across 61 sites in 3 countries.

Detailed Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Chemoprotective drugs, such as enalapril, may protect normal cells from the toxic effects of chemotherapy. It is not known whether enalapril is more effective than a placebo in treating heart damage in patients who received anthracycline chemotherapy for childhood cancer. PURPOSE: Randomized double-blinded phase III trial to compare the effectiveness of enalapril with a placebo in treating heart damage in patients who received anthracycline chemotherapy for childhood cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, Switzerland, United States

Timeline

Phase 3CompletedFinished
2000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMar 1, 2004
Enrollment StartSep 1, 2000
Primary CompletionJul 1, 2003
Study CompletionMar 1, 2007
TodayJul 2, 2026
Enrollment to primary: 2.8 yearsPosted 22.3 years ago

Interventions

enalapril maleatedrug

quality-of-life assessmentprocedure