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NCT00624065 · ClinicalTrials.gov registry record · Phase 3

Research Study To Test Carvedilol CR + Lisinopril Versus Lisinopril + Placebo In Patients With High Blood Pressure

A Phase 3 study, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 3
Development phase
348
Enrollment target

NCT00624065: Completed Phase 3 study, sponsored by GlaxoSmithKline.

NCT00624065 is a Phase 3 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 348 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00624065, a Phase 3 study, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 3
Development phase
348 participants
Enrollment target

Study Summary

Randomized, double-blind, parallel group, multicenter study of subjects with Stage 1 or 2 essential hypertension who are not at target blood pressure (\<140/90mmHg) at Baseline. Subjects will be randomized to receive either carvedilol CR + lisinopril or lisinopril + placebo. Subjects will be uptitrated over a 6 week period until target blood pressure (\<140/90mmHg) is met. The primary objective of the study is to compare the proportion of subjects who achieve target blood pressure after 6 weeks of treatment.

Primary Outcome

Sitting cuff blood pressure was calculated as the mean of three measurements taken approximately 2 minutes apart, and before the morning dose.

Interventions

  • DRUG carvedilol controlled release/lisinopril
  • DRUG lisinopril + placebo

Trial Details

FieldValue
Enrollment Target 348 participants
Start Date 2008-03
Est. Completion 2008-08
Phase Phase 3
GlaxoSmithKline

1,345 total trials

What the finished NCT00624065 record still lists

NCT00624065 is an interventional study that assigns participants to a tested intervention. The registered 348 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (55% lower).

The record links to 0 conditions, and to 2 interventions - of which carvedilol controlled release/lisinopril is the first listed.

NCT00624065 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00624065 about?

NCT00624065 is a clinical study titled "Research Study To Test Carvedilol CR + Lisinopril Versus Lisinopril + Placebo In Patients With High Blood Pressure". Randomized, double-blind, parallel group, multicenter study of subjects with Stage 1 or 2 essential hypertension who are not at target blood pressure (\<140/90mmHg) at Baseline. Subjects will be randomized to receive either carvedilol CR + lisinopril or lisinopril + placebo. Subjects will be uptitra...

What is the current status of trial NCT00624065?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 348 participants. The study started on 2008-03. Estimated completion is 2008-08.

What interventions are being tested in trial NCT00624065?

The interventions under investigation include: carvedilol controlled release/lisinopril (DRUG), lisinopril + placebo (DRUG).

Who is sponsoring clinical trial NCT00624065?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00624065's enrollment target sits among peer trials

348 1045th of 2000 higher than 953 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00624065, the US trial registry maintained by the National Library of Medicine. NCT00624065 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.