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Active, not recruiting Phase 3 Interventional

Amiodarone and N-Acetylcysteine or Amiodarone Alone for Preventing Atrial Fibrillation After Thoracic Surgery

ClinicalTrials.gov ID: NCT02750319

Public ClinicalTrials.gov record NCT02750319. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 7, 2026, 9:06 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Controlled Trial of Combined Amiodarone and N-Acetylcysteine Versus Amiodarone Plus Placebo for the Prevention of Atrial Fibrillation in High Risk Patients Undergoing Thoracic Surgery

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This trial will be comparing the combination of amiodarone and NAC (n=122) to amiodarone alone and NAC matched placebo (n=122) to determine the rates with which sustained (lasting \>30 seconds) or clinically significant POAF is reduced in high risk patients within 7 days after major thoracic surgery.

Study identification

NCT ID
NCT02750319
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Enrollment
184 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 2016 (Actual)
Primary completion
Apr 2027 (Estimated)
Completion
Apr 2027 (Estimated)
Last update posted
May 19, 2026

2016 – 2027

United States locations

U.S. sites
9
U.S. states
3
U.S. cities
9
Facility City State ZIP Site status
University of Washington School of Medicine in St. Louis St Louis Missouri 63110 —
Memorial Sloan Kettering Basking Ridge (Consent only) Basking Ridge New Jersey — —
Memorial Sloan Kettering Monmouth (Consent only) Middletown New Jersey 07748 —
Memorial Sloan Kettering Bergen (Consent only) Montvale New Jersey 07645 —
Memorial Sloan Kettering Commack (Consent only) Commack New York 11725 —
Memorial Sloan Kettering Westchester (Consent only) Harrison New York 10604 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Memorial Sloan Kettering Rockville Centre (Consent only) Rockville Centre New York 11570 —
Memorial Sloan Kettering Nassau (Consent only) Uniondale New York 11553 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02750319, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 19, 2026 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02750319 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →