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

NCT00887510 · ClinicalTrials.gov registry record · Phase 4

Metabolic Effects of Antihypertensive Drugs on People With Metabolic Syndrome (The MEAD Study)

A Phase 4 study, sponsored by University of Florida.

Completed
Registry status
Phase 4
Development phase
24
Enrollment target

NCT00887510: Completed Phase 4 study, sponsored by University of Florida.

NCT00887510 is a Phase 4 study that has completed, run by University of Florida. The registered enrollment target is 24 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00887510, a Phase 4 study, has completed, sponsored by University of Florida.

COMPLETED
Registry status
Phase 4
Development phase
24 participants
Enrollment target

Study Summary

High blood pressure, also referred to as hypertension, is a blood pressure level of 140/90 mm Hg or higher. Along with lifestyle changes, various medications are currently used to treat people with hypertension. Some of these medications, however, may affect the way the body handles sugar, essentially preventing the body from breaking down sugar and predisposing people to developing diabetes. People who have metabolic syndrome-a condition primarily characterized by an increased waist measurement, abnormal blood lipid levels, hypertension, and high blood sugar levels-are already at risk of developing diabetes. In these people, taking the antihypertensive medications that prevent sugar breakdown may further increase their risk of diabetes. The purpose of this study is to gain an understanding of how people with metabolic syndrome respond to antihypertensive medications that alter the body's ability to break down sugar.

Primary Outcome

Comparing the change in OGTT AUC rand 1 visit4-visit 3 with rand 2 visit 3-2. This allows for understanding the effects of addition of trandolapril to 12 weeks of HCTZ compared with addition of HCTZ to 12 weeks of trandolapril. This is the primary outcome of the study.

Interventions

  • DRUG Hydrochlorothiazide
  • DRUG Trandolapril

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2007-05
Est. Completion 2009-11
Phase Phase 4
University of Florida

1,106 total trials

What the finished NCT00887510 record still lists

NCT00887510 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which Hydrochlorothiazide is the first listed.

NCT00887510 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00887510 about?

NCT00887510 is a clinical study titled "Metabolic Effects of Antihypertensive Drugs on People With Metabolic Syndrome (The MEAD Study)". High blood pressure, also referred to as hypertension, is a blood pressure level of 140/90 mm Hg or higher. Along with lifestyle changes, various medications are currently used to treat people with hypertension. Some of these medications, however, may affect the way the body handles sugar, essential...

What is the current status of trial NCT00887510?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 24 participants. The study started on 2007-05. Estimated completion is 2009-11.

What interventions are being tested in trial NCT00887510?

The interventions under investigation include: Hydrochlorothiazide (DRUG), Trandolapril (DRUG).

Who is sponsoring clinical trial NCT00887510?

This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00887510's enrollment target sits among peer trials

24 1699th of 2000 higher than 276 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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

  • NCT02331979 · 24 participants · NA

    Improving Bladder Function in SCI by Neuromodulation

  • NCT03096197 · 24 participants · NA

    Exoskeleton and Spinal Cord Stimulation for SCI

  • NCT03223922 · 24 participants · NA

    Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases

  • NCT03326921 · 24 participants · Phase 1

    HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant

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 NCT00887510, the US trial registry maintained by the National Library of Medicine. NCT00887510 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.