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

NCT01502787 · ClinicalTrials.gov registry record · Phase 4

Comparison of Nebivolol and Metoprolol With Exercise and Angiotensin II in Hypertensive Patients

A Phase 4 study, sponsored by University of Texas Southwestern Medical Center.

Completed
Registry status
Phase 4
Development phase
46
Enrollment target

NCT01502787: Completed Phase 4 study, sponsored by University of Texas Southwestern Medical Center.

NCT01502787 is a Phase 4 study that has completed, run by University of Texas Southwestern Medical Center. The registered enrollment target is 46 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01502787, a Phase 4 study, has completed, sponsored by University of Texas Southwestern Medical Center.

COMPLETED
Registry status
Phase 4
Development phase
46 participants
Enrollment target

Study Summary

The purpose of this study is to determine if Nebivolol a) attenuates the angiotensin II (Ang II)-induced increase in oxidative stress, thereby attenuating Ang II-induced vasoconstriction; and b) attenuates sympathetic mediated vasoconstriction during exercise, thereby reducing functional skeletal muscle ischemia in hypertensive patients.

Interventions

  • DRUG Nebivolol
  • DRUG Metoprolol succinate
  • PROCEDURE Microneurography
  • PROCEDURE Rhythmic handgrip exercise
  • PROCEDURE Forearm blood flow

Trial Details

FieldValue
Enrollment Target 46 participants
Start Date 2009-04
Est. Completion 2013-06
Phase Phase 4

What the finished NCT01502787 record still lists

NCT01502787 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 46 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (91% lower).

The record links to 0 conditions, and to 5 interventions - of which Nebivolol is the first listed.

NCT01502787 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01502787 about?

NCT01502787 is a clinical study titled "Comparison of Nebivolol and Metoprolol With Exercise and Angiotensin II in Hypertensive Patients". The purpose of this study is to determine if Nebivolol a) attenuates the angiotensin II (Ang II)-induced increase in oxidative stress, thereby attenuating Ang II-induced vasoconstriction; and b) attenuates sympathetic mediated vasoconstriction during exercise, thereby reducing functional skeletal mu...

What is the current status of trial NCT01502787?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 46 participants. The study started on 2009-04. Estimated completion is 2013-06.

What interventions are being tested in trial NCT01502787?

The interventions under investigation include: Nebivolol (DRUG), Metoprolol succinate (DRUG), Microneurography (PROCEDURE), Rhythmic handgrip exercise (PROCEDURE), Forearm blood flow (PROCEDURE).

Who is sponsoring clinical trial NCT01502787?

This trial is sponsored by University of Texas Southwestern Medical Center, which has 837 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01502787's enrollment target sits among peer trials

46 1348th of 2000 higher than 647 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

  • NCT01890590 · 46 participants · NA

    A Phase II Study of Cyberknife Radiosurgery for Renal Cell Carcinoma

  • NCT03191149 · 46 participants · Phase 2

    Testing Osimertinib as a Treatment for Lung Cancers With an EGFR Exon 20 Change

  • NCT03510208 · 46 participants · Phase 1

    Panitumumab-IRDye800 in Diagnosing Participants With Malignant Glioma Undergoing Surgery

  • NCT04048278 · 46 participants · Early Phase 1

    Lidocaine Infusion in Pancreatic Cancer

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 NCT01502787, the US trial registry maintained by the National Library of Medicine. NCT01502787 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.