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NCT02293096 · ClinicalTrials.gov registry record · NA

Pharmacogenetic Prediction of Metoprolol Effectiveness

A NA study, sponsored by University of Colorado, Denver.

Terminated
Registry status
NA
Development phase
462
Enrollment target

NCT02293096: Clinical Trial NA study, sponsored by University of Colorado, Denver.

NCT02293096 is a NA study that was terminated before completion, run by University of Colorado, Denver. The registered enrollment target is 462 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02293096, a NA study, was terminated before completion, sponsored by University of Colorado, Denver.

TERMINATED
Registry status
NA
Development phase
462 participants
Enrollment target

Study Summary

The investigators will prospectively follow a population of patients with uncontrolled high blood pressure beginning metoprolol succinate therapy to determine the drug effect in an observational clinical trial. The investigators will determine each individual's genotype for both CYP2D6 and Adrenoceptor Beta 1 (ADRB1). Metabolomic markers will be identified to determine if specific metabolites are associated with drug response. The investigators' overall objective is to determine if genetics predicts metoprolol succinate response better than clinical factors such as age, race, body mass index, dose, and medication co-ingestion.

Primary Outcome

Participants with at least a 10% decrease in SBP

Interventions

  • GENETIC Genotyping
  • DRUG metoprolol succinate
  • PROCEDURE CYP2D6 Phenotyping

Trial Details

FieldValue
Enrollment Target 462 participants
Start Date 2014-09
Est. Completion 2017-08-23
Phase NA
University of Colorado, Denver

1,283 total trials

Why NCT02293096 stopped before completion

NCT02293096 is an interventional study that assigns participants to a tested intervention. The registered 462 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (67% lower).

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

NCT02293096 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02293096 about?

NCT02293096 is a clinical study titled "Pharmacogenetic Prediction of Metoprolol Effectiveness". The investigators will prospectively follow a population of patients with uncontrolled high blood pressure beginning metoprolol succinate therapy to determine the drug effect in an observational clinical trial. The investigators will determine each individual's genotype for both CYP2D6 and Adrenocep...

What is the current status of trial NCT02293096?

This trial is currently terminated. It is a NA study. The enrollment target is 462 participants. The study started on 2014-09. Estimated completion is 2017-08-23.

What interventions are being tested in trial NCT02293096?

The interventions under investigation include: Genotyping (GENETIC), metoprolol succinate (DRUG), CYP2D6 Phenotyping (PROCEDURE).

Who is sponsoring clinical trial NCT02293096?

This trial is sponsored by University of Colorado, Denver, which has 1,283 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02293096's enrollment target sits among peer trials

462 222nd of 2000 higher than 1,779 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

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Source: ClinicalTrials.gov NCT02293096, the US trial registry maintained by the National Library of Medicine. NCT02293096 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.