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Rapid Versus Prolonged Inpatient Up-Titration of Captopril

NCT00742040 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2008-08-27

No results posted yet for this study

Summary

The primary objective of this study is to establish a safe and effective method of up-titration of captopril for hospital inpatients.

Conditions

Interventions

DRUG

Captopril

A rapid 3-day up-titration protocol

DRUG

Captopril

A slower 9-day up-titration protocol

Sponsors & Collaborators

  • The Hospital for Sick Children

    lead OTHER

Principal Investigators

  • Paul Kantor, MD · The Hospital for Sick Children

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-08-31
Primary Completion
2009-08-31
Completion
2009-12-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00742040 on ClinicalTrials.gov