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Clinical Trials in Turkey / NCT07172529
Active, not recruiting Observational

Pulmonary Function, Muscle Strength, and Functional Capacity in Minimally Invasive Cardiac Surgery

NCT07172529 · tracked via the Priya Life Science Turkey tracker
Sponsor
Zehra Can Karahan
Phase
Observational
Started
2024-05-01
Last updated
2025-09-15

Condition(s) studied

Cardiac SurgeryMuscle Weakness | PatientPulmonary FunctionFunctional Capacity

Study summary

The goal of this observational study is to evaluate pulmonary function, respiratory muscle strength, peripheral muscle strength, and functional capacity in adult patients undergoing either minimally invasive cardiac surgery (via mini-thoracotomy) or conventional sternotomy for coronary artery bypass grafting (CABG) at Gülhane Training and Research Hospital.The main questions it aims to answer are:

Does minimally invasive cardiac surgery preserve pulmonary function better than conventional sternotomy? Does minimally invasive cardiac surgery result in less respiratory and peripheral muscle weakness compared to conventional sternotomy? Researchers will compare patients undergoing minimally invasive surgery with those undergoing conventional sternotomy to determine differences in pulmonary function, respiratory muscle strength, peripheral muscle strength, and functional capacity.

Participants will:

Undergo preoperative and postoperative (day 4) assessments including spirometry, inspiratory/expiratory mouth pressure measurements, and peripheral muscle strength testing (handgrip, shoulder flexion/abduction, hip flexion, knee extension).

Perform functional capacity tests (30-second sit-to-stand test, 6-minute walk test).

Complete questionnaires assessing pain (McGill Pain Questionnaire) and fear of movement (Tampa Scale of Kinesiophobia).

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18-80 years * Scheduled for elective cardiac surgery via either minimally invasive approach (mini-thoracotomy) or conventional sternotomy at Gülhane Training and Research Hospital * Able to provide written informed consent Exclusion Criteria: * Previous history of cardiac surgery * Presence of orthopedic or neurological disorders affecting mobility or muscle strength * Postoperative cerebrovascular event * Requirement for mechanical ventilation \> 24 hours postoperatively * Intensive care unit stay \> 48 hours

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Atilim University Ankara Turkey (Türkiye)

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07172529 on ClinicalTrials.gov ↗ ← All trials in Turkey