Impact of Left Atrial Function on Postoperative Atrial Fibrillation
NCT ID: NCT00646997
Last Updated: 2008-06-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
80 participants
OBSERVATIONAL
2008-03-31
2008-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CROSSOVER
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1
Patients with postoperative atrial fibrillation
No interventions assigned to this group
2
Patients without postoperative atrial fibrillation.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 2Patients with a decision of undergoing elective coronary artery bypass greft operation
* 3Sinus rhythm in electrocardiography
Exclusion Criteria
* 2Having prosthetic valve
* 3CABG accompanied by other cardiac interventions (such as valvular surgery, ASD closure...etc)
* 4Left ventricular l ejection fraction \<40%
* 5Mild to moderate mitral stenosis or regurgitation
* 6Having atrial fibrillation or a history of atrial fibrillation attach during the last two weeks.
* 7Congenital heart disease
* 8Chronic liver disease
* 9Chronic renal disease
* 10Malignancy
30 Years
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Florence Nightingale Hospital, Istanbul
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
T.C. Istanbul Bilim University, Florence Nightingale Hospital
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Saide Aytekin, Professor
Role: STUDY_DIRECTOR
T.C. Istanbul Bilim University, Florence Nightingale Hospital, Division of Cardiology
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
TC.Istanbul Bilim University, Florence Nightingale Hospital, Division of Cardiology
Istanbul, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
1-Leung JM, Bellows WH, Schiller NB. Impairment of left atrial function predicts post-operative atrial fibrillation after coronary artery bypass graft surgery. European H J. 2004,25,1836-1844 2-Nakai T , Lee R, Schiller N, et al. The relative importance of left atrial function versus dimension in predicting atrial fibrilation after coronary bypass graft surgery. Am H Journal. 2002; 143:181-6
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
YT1977/2
Identifier Type: -
Identifier Source: org_study_id