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NCT00127712 · ClinicalTrials.gov registry record · Phase 4

Prevention of Atrial Fibrillation Following Noncardiac Thoracic Surgery

A Phase 4 study, sponsored by Indiana University.

Completed
Registry status
Phase 4
Development phase
130
Enrollment target

NCT00127712: Completed Phase 4 study, sponsored by Indiana University.

NCT00127712 is a Phase 4 study that has completed, run by Indiana University. The registered enrollment target is 130 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (75% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00127712, a Phase 4 study, has completed, sponsored by Indiana University.

COMPLETED
Registry status
Phase 4
Development phase
130 participants
Enrollment target

Study Summary

The investigators hypothesize that the medication amiodarone decreases the incidence of atrial fibrillation (AF) following non-cardiac open-chest surgery. Their specific aims are to: * Determine the effectiveness of amiodarone for the prevention of AF following non-cardiac open-chest surgery; * Determine the influence of the prevention of AF following non-cardiac thoracic surgery on post-surgical duration of stay in the Intensive Care Unit (ICU); post-surgical duration of stay in a hospital unit that employs cardiac monitoring; and duration of post-surgical hospital stay; and * Determine the safety of amiodarone for the prevention of AF following non-cardiac open-chest surgery.

Interventions

  • DRUG Amiodarone

Trial Details

FieldValue
Enrollment Target 130 participants
Start Date 2004-09
Est. Completion 2008-02
Phase Phase 4
Indiana University

890 total trials

What the finished NCT00127712 record still lists

NCT00127712 is an interventional study that assigns participants to a tested intervention. The registered 130 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (75% lower).

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

NCT00127712 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00127712 about?

NCT00127712 is a clinical study titled "Prevention of Atrial Fibrillation Following Noncardiac Thoracic Surgery". The investigators hypothesize that the medication amiodarone decreases the incidence of atrial fibrillation (AF) following non-cardiac open-chest surgery. Their specific aims are to: * Determine the effectiveness of amiodarone for the prevention of AF following non-cardiac open-chest surgery; * Det...

What is the current status of trial NCT00127712?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 130 participants. The study started on 2004-09. Estimated completion is 2008-02.

What interventions are being tested in trial NCT00127712?

The interventions under investigation include: Amiodarone (DRUG).

Who is sponsoring clinical trial NCT00127712?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00127712's enrollment target sits among peer trials

130 622nd of 2000 higher than 1,370 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

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Source: ClinicalTrials.gov NCT00127712, the US trial registry maintained by the National Library of Medicine. NCT00127712 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.