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NCT00168779 · ClinicalTrials.gov registry record · Phase 4

Randomized, Double-Blind, Placebo-Controlled, Forced-Titration, Comparing Telmisartan vs Valsartan. Taken Orally for Eight Weeks in Patients With Stage 1 and Stage 2 Hypertension

A Phase 4 study, sponsored by Boehringer Ingelheim.

Completed
Registry status
Phase 4
Development phase
1,185
Enrollment target

NCT00168779 is a Phase 4 study that has completed, run by Boehringer Ingelheim. The registered enrollment target is 1,185 participants.

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The verdict

NCT00168779, a Phase 4 study, has completed, sponsored by Boehringer Ingelheim.

COMPLETED
Registry status
Phase 4
Development phase
1,185 participants
Enrollment target

Study Summary

The primary objective of this study is to compare the effectiveness of telmisartan 80 mg / hydrochlorothiazide 25 mg \[Micardis HCT\] to valsartan 160 mg / hydrochlorothiazide 25 mg \[Diovan HCT\] and placebo in the treatment of Stage 1 and Stage 2 hypertension.

Interventions

  • DRUG placebo
  • DRUG telmisartan 80 mg / hydrochlorothiazide 25 mg
  • DRUG valsartan 160 mg / hydrochlorothiazide 25 mg

Trial Details

FieldValue
Enrollment Target 1,185 participants
Start Date 2005-09
Est. Completion 2006-07
Phase Phase 4

Sponsor

Boehringer Ingelheim

515 total trials

What the Registry Record Tells You About NCT00168779

The ClinicalTrials.gov registry entry for NCT00168779 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 1,185 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boehringer Ingelheim, which has 515 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which placebo is the first listed.

NCT00168779 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00168779 about?

NCT00168779 is a clinical study titled "Randomized, Double-Blind, Placebo-Controlled, Forced-Titration, Comparing Telmisartan vs Valsartan. Taken Orally for Eight Weeks in Patients With Stage 1 and Stage 2 Hypertension". The primary objective of this study is to compare the effectiveness of telmisartan 80 mg / hydrochlorothiazide 25 mg \[Micardis HCT\] to valsartan 160 mg / hydrochlorothiazide 25 mg \[Diovan HCT\] and placebo in the treatment of Stage 1 and Stage 2 hypertension.

What is the current status of trial NCT00168779?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 1,185 participants. The study started on 2005-09. Estimated completion is 2006-07.

What interventions are being tested in trial NCT00168779?

The interventions under investigation include: placebo (DRUG), telmisartan 80 mg / hydrochlorothiazide 25 mg (DRUG), valsartan 160 mg / hydrochlorothiazide 25 mg (DRUG).

Who is sponsoring clinical trial NCT00168779?

This trial is sponsored by Boehringer Ingelheim, which has 515 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.