Completed

Evaluation of Factors Affecting Extubation Times in Postoperative Congenital Cardiovascular Surgeries: A Randomized Prospective Study

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Congenital Abnormalities+3

+ Cardiovascular Diseases

+ Heart Defects, Congenital

See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: May 2020
See protocol details

Summary

Principal SponsorBursa Yuksek Ihtisas Training and Research Hospital
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: May 1, 2020

Actual date on which the first participant was enrolled.

This study focuses on children who undergo heart surgery for critical congenital heart disease. The goal is to understand how to reduce the need for mechanical ventilation (breathing machines) after surgery. This is important because less time on a ventilator can lead to fewer complications, better recovery, and more efficient use of healthcare resources. The researchers are looking at various factors such as patient characteristics, surgery details, and post-surgery care that might influence the time it takes for a child to be safely removed from the ventilator.

Official TitleEvaluation of Factors Affecting Extubation Times in Postoperative Congenital Cardiovascular Surgeries: A Randomized Prospective Study
NCT05332860
Principal SponsorBursa Yuksek Ihtisas Training and Research Hospital
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

72 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Congenital AbnormalitiesCardiovascular DiseasesHeart Defects, CongenitalHeart DiseasesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesCardiovascular Abnormalities

Criteria

Inclusion Criteria: * elective or emergency patients * aged 0-18 who are scheduled for congenital heart surgery Exclusion Criteria: -in patients who died during the operation

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Bursa Training and Research Hospital

Bursa, Turkey (Türkiye)Open Bursa Training and Research Hospital in Google Maps
CompletedOne Study Center