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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 May 20, 2026, 6:26 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. 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

Study identification

NCT ID
NCT02750319
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Memorial Sloan Kettering Cancer Center
Other
Enrollment
184 participants

Conditions and interventions

Interventions

  • Amiodarone Drug
  • N-Acetylcysteine Drug
  • Placebo Drug

Drug

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
Mar 31, 2016
Primary completion
Mar 31, 2027
Completion
Mar 31, 2027
Last update posted
May 18, 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 18, 2026 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02750319 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →