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

NCT01558128 · ClinicalTrials.gov registry record · NA

Combined Amiodarone and Electrical Cardioversion for Postoperative Atrial Fibrillation After Cardiac Surgery

A NA study, sponsored by Weill Medical College of Cornell University.

Terminated
Registry status
NA
Development phase
1
Enrollment target

NCT01558128 is a NA study that was terminated before completion, run by Weill Medical College of Cornell University. The registered enrollment target is 1 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01558128, a NA study, was terminated before completion, sponsored by Weill Medical College of Cornell University.

TERMINATED
Registry status
NA
Development phase
1 participants
Enrollment target

Study Summary

To determine the efficacy of cardioversion and amiodarone for cardiac patients who develop postoperative atrial fibrillation

Interventions

  • DRUG Amiodarone
  • PROCEDURE Cardioversion

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2012-03
Est. Completion 2013-03
Phase NA

What the Registry Record Tells You About NCT01558128

The ClinicalTrials.gov registry entry for NCT01558128 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 1 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Weill Medical College of Cornell University, which has 701 total studies on file at ClinicalTrials.gov.

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

NCT01558128 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01558128 about?

NCT01558128 is a clinical study titled "Combined Amiodarone and Electrical Cardioversion for Postoperative Atrial Fibrillation After Cardiac Surgery". To determine the efficacy of cardioversion and amiodarone for cardiac patients who develop postoperative atrial fibrillation

What is the current status of trial NCT01558128?

This trial is currently terminated. It is a NA study. The enrollment target is 1 participants. The study started on 2012-03. Estimated completion is 2013-03.

What interventions are being tested in trial NCT01558128?

The interventions under investigation include: Amiodarone (DRUG), Cardioversion (PROCEDURE).

Who is sponsoring clinical trial NCT01558128?

This trial is sponsored by Weill Medical College of Cornell University, which has 701 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.