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UNKNOWNNCT05448521

Postoperative Lactate and Atrial Fibrillation After CABG

Postoperative atrial fibrillation (POAF) is associated with increased mortality and morbidity in patients undergoing isolated coronary artery bypass grafting (CABG). It has been estimated that 5-40% o...

Lead sponsor: Başakşehir Çam & Sakura City Hospital•1 locations•View source on ClinicalTrials.gov

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Contacts

Zeki Temizturk, MD

CONTACT

902129096000 [email protected]

Ahmet Can Topcu, MD

CONTACT

902165001500 [email protected]

Sponsors

Lead Sponsor

Başakşehir Çam & Sakura City Hospital

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Undergoing isolated CABG
•Age \>18 years

Exclusion Criteria

•Age \<18 years
•Pregnancy
•History of paroxysmal atrial fibrillation prior to surgery
•Undergoing concomitant procedures (e.g., CABG + valve surgery)
•Any preoperative cardiac rhythm other than normal sinus rhythm
•More than mild cardiac valve stenosis or insufficiency

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: October 10, 2022Terms

Trial snapshot

StatusUNKNOWN

Phase—

Enrollment250

Start dateAug 2022

Last updatedOct 10, 2022

Condition

Coronary Artery Disease Atrial Fibrillation

Locations shown

Basaksehir Cam Sakura City Hospital

Istanbul

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: October 10, 2022Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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