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NCT01202175 · ClinicalTrials.gov registry record · Phase 4

Effects of the Beta-blocker Nebivolol (Bystolic) on Subjects With High Normal Blood Pressure and/or a Family History of Hypertension

A Phase 4 study, sponsored by University of California, San Diego.

Completed
Registry status
Phase 4
Development phase
50
Enrollment target

NCT01202175 is a Phase 4 study that has completed, run by University of California, San Diego. The registered enrollment target is 50 participants.

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The verdict

NCT01202175, a Phase 4 study, has completed, sponsored by University of California, San Diego.

COMPLETED
Registry status
Phase 4
Development phase
50 participants
Enrollment target

Study Summary

The investigators aim to evaluate subjects at high risk of future development of hypertension, those with a family history of hypertension and/or that already have high normal(SBP 120-139 mmHg or DBP 80-89 mmHg) blood pressure. The investigators plan to investigate whether these subjects have the same markers (such as microscopic protein in the urine or C-reactive protein in the blood) in the blood and urine that people with high blood pressure have, and whether they are improved before and after taking the beta-blocker nebivolol.

Interventions

  • DRUG Nebivolol

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2010-07
Est. Completion 2013-06
Phase Phase 4

Sponsor

University of California, San Diego

775 total trials

What the Registry Record Tells You About NCT01202175

The ClinicalTrials.gov registry entry for NCT01202175 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Diego, which has 775 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Nebivolol is the first listed.

NCT01202175 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01202175 about?

NCT01202175 is a clinical study titled "Effects of the Beta-blocker Nebivolol (Bystolic) on Subjects With High Normal Blood Pressure and/or a Family History of Hypertension". The investigators aim to evaluate subjects at high risk of future development of hypertension, those with a family history of hypertension and/or that already have high normal(SBP 120-139 mmHg or DBP 80-89 mmHg) blood pressure. The investigators plan to investigate whether these subjects have the sa...

What is the current status of trial NCT01202175?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2010-07. Estimated completion is 2013-06.

What interventions are being tested in trial NCT01202175?

The interventions under investigation include: Nebivolol (DRUG).

Who is sponsoring clinical trial NCT01202175?

This trial is sponsored by University of California, San Diego, which has 775 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.