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

NCT00806390 · ClinicalTrials.gov registry record · Phase 4

Prevention of Anthracycline or Trastuzumab Induced Cardiomyopathy by Metoprolol

A Phase 4 study, sponsored by University of Maryland, Baltimore.

Terminated
Registry status
Phase 4
Development phase
15
Enrollment target

NCT00806390: Clinical Trial Phase 4 study, sponsored by University of Maryland, Baltimore.

NCT00806390 is a Phase 4 study that was terminated before completion, run by University of Maryland, Baltimore. The registered enrollment target is 15 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00806390, a Phase 4 study, was terminated before completion, sponsored by University of Maryland, Baltimore.

TERMINATED
Registry status
Phase 4
Development phase
15 participants
Enrollment target

Study Summary

The primary objective of this study is to investigate whether giving prophylactic metoprolol prior to and during anthracycline or trastuzumab therapy will decrease the incidence of anthracycline-induced cardiomyopathy. Patients are randomized to receive metoprolol or no treatment prior to anthracycline or trastuzumab treatment. The ejection fraction, as measured by nuclear ventriculography is measured before and after treatment.

Primary Outcome

Because of the inability to enroll an adequate number of patients, (only 15 out of a planned 50) no data analysis was collected or performed.

Interventions

  • DRUG Metoprolol

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2008-07
Est. Completion 2012-06
Phase Phase 4
University of Maryland, Baltimore

560 total trials

Why NCT00806390 stopped before completion

NCT00806390 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (97% lower).

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

NCT00806390 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00806390 about?

NCT00806390 is a clinical study titled "Prevention of Anthracycline or Trastuzumab Induced Cardiomyopathy by Metoprolol". The primary objective of this study is to investigate whether giving prophylactic metoprolol prior to and during anthracycline or trastuzumab therapy will decrease the incidence of anthracycline-induced cardiomyopathy. Patients are randomized to receive metoprolol or no treatment prior to anthracycl...

What is the current status of trial NCT00806390?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 15 participants. The study started on 2008-07. Estimated completion is 2012-06.

What interventions are being tested in trial NCT00806390?

The interventions under investigation include: Metoprolol (DRUG).

Who is sponsoring clinical trial NCT00806390?

This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00806390's enrollment target sits among peer trials

15 1880th of 2000 higher than 100 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

  • NCT01889381 · 15 participants · Phase 2

    Human Craniomaxillofacial Allotransplantation

  • NCT02530073 · 15 participants · NA

    Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) for CDH

  • NCT02535936 · 15 participants · NA

    Cortical Plasticity in Spastic Diplegia After Selective Dorsal Rhizotomy

  • NCT02918474 · 15 participants · NA

    Decision Making Tool in Supporting Decision Making in Contralateral Prophylactic Mastectomy in Patients With Newly Diagnosed Breast 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 NCT00806390, the US trial registry maintained by the National Library of Medicine. NCT00806390 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.