Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00095550 · ClinicalTrials.gov registry record · Phase 3

Irbesartan/Hydrochlorothiazide (HCTZ) Combination Therapy for Patients With Moderate Hypertension

A Phase 3 study, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 3
Development phase
496
Enrollment target

NCT00095550: Completed Phase 3 study, sponsored by Bristol-Myers Squibb.

NCT00095550 is a Phase 3 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 496 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (36% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00095550, a Phase 3 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 3
Development phase
496 participants
Enrollment target

Study Summary

The purpose of this clinical research is to learn if moderate hypertension can be better controlled by initially treating with a combination of drugs (Irbesartan/HCTZ), in patients who are unlikely to achieve blood pressure (B/P) control with only one drug. In addition, the study will also evaluate the safety and tolerability of the drugs.

Interventions

  • DRUG Irbesartan/HCTZ
  • DRUG Irbesartan monotherapy
  • DRUG HCTZ monotherapy

Trial Details

FieldValue
Enrollment Target 496 participants
Start Date 2004-10
Est. Completion 2005-06
Phase Phase 3
Bristol-Myers Squibb

1,025 total trials

What the finished NCT00095550 record still lists

NCT00095550 is an interventional study that assigns participants to a tested intervention. The registered 496 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 (36% lower).

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

NCT00095550 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00095550 about?

NCT00095550 is a clinical study titled "Irbesartan/Hydrochlorothiazide (HCTZ) Combination Therapy for Patients With Moderate Hypertension". The purpose of this clinical research is to learn if moderate hypertension can be better controlled by initially treating with a combination of drugs (Irbesartan/HCTZ), in patients who are unlikely to achieve blood pressure (B/P) control with only one drug. In addition, the study will also evaluate ...

What is the current status of trial NCT00095550?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 496 participants. The study started on 2004-10. Estimated completion is 2005-06.

What interventions are being tested in trial NCT00095550?

The interventions under investigation include: Irbesartan/HCTZ (DRUG), Irbesartan monotherapy (DRUG), HCTZ monotherapy (DRUG).

Who is sponsoring clinical trial NCT00095550?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00095550's enrollment target sits among peer trials

496 776th of 2000 higher than 1,223 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05283720 · 496 participants · Phase 2

    A Study to Evaluate Adverse Events and Change in Disease Activity of Subcutaneous (SC) Epcoritamab in Combination With Oral and Intravenous Anti-Neoplastic Agents in Adult Participants With Non-Hodgkin Lymphoma

  • NCT06417775 · 496 participants · Phase 3

    Study of Oral Ubrogepant to Assess Adverse Events and Change in Disease Activity in Adult Participants With Menstrual Migraine

  • NCT06778447 · 496 participants · NA

    Clinical Trial Evaluating the Safety and Efficacy of Nucleus Pulposus Allograft in Participants With Degenerative Disc Disease

  • NCT03175224 · 497 participants · Phase 2

    APL-101 Study of Subjects With NSCLC With c-Met EXON 14 Skip Mutations and c-Met Dysregulation Advanced Solid Tumors

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00095550, the US trial registry maintained by the National Library of Medicine. NCT00095550 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.