CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed
Drug / intervention
SCH-58235 +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/NCT00099996
NCT00099996Phase 3Completed

A Study to Assess Adding Ezetimibe 30 mg to Ongoing Treatment With Ezetimibe 10 mg in Patients With Homozygous Sitosterolemia

National Heart, Lung, and Blood Institute (NHLBI)·interventional·Posted Dec 22, 2004·Updated Mar 4, 2008

In Brief

A Phase 3 clinical trial evaluating SCH-58235 and Ezetimibe for Heart Diseases and Metabolism, Inborn Errors. Completed, across 1 site.

Detailed Summary

This study will test the safety and effectiveness of 40 mg of ezetimibe (Zetia ) daily in lowering blood levels of cholesterol and of the plant sterols sitosterol and campesterol in patients with homozygous sitosterolemia, an inherited disorder of sterol metabolism. (Sterols are alcohol substances found in animal and plant fats.) In this disorder, an excess of many plant sterols is absorbed and not enough excreted. Patients can develop atherosclerosis and coronary heart disease as early as childhood, as well as other problems including arthritis, arthralgia, and tendon xanthomas (lipid deposits). Current treatment consists of ezetimibe 10 mg, dietary restriction of plant and shellfish sterols, and bile salt binding resins. Ezetimibe is a cholesterol-lowering drug that inhibits intestinal absorption of cholesterol and structurally related plant sterols across the intestinal wall. Patients with homozygous sitosterolemia who are between 18 and 85 years of age have completed NHLBI's 1-year study of ezetimibe at 10 mg a day may be eligible for this study. All participants maintain their current stable diet and take a 10-mg pill of ezetimibe daily for 26 weeks. They are also randomly selected to take either an additional 30-mg pill of ezetimibe or a placebo (look-alike pill with no active ingredients). Patients fast for at least 12 hours before each of 6 visits scheduled during the course of the study. At these visits, patients undergo some or all of the following procedures for monitoring their health and evaluating their response to treatment: * Medical history and review of medications * Physical examination * Measurement of vital signs (pulse rate, blood pressure, breathing rate and temperature) * Review of dietary maintenance * Measurements of height, weight, and waist circumference * Measurement (with ruler) and photographs of non-Achilles xanthoma * X-ray of Achilles tendon * Blood draw and urine collection * Pregnancy test for women of childbearing potential

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 3CompletedFinished
20052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedDec 22, 2004
Enrollment StartDec 1, 2004
Study CompletionDec 1, 2005
TodayJul 2, 2026
Posted 21.5 years ago

Interventions

SCH-58235drug

Ezetimibedrug