Status:
COMPLETED
Intraocular Pressure in Patients Undergoing Coronary Artery Bypass Graft Surgery With Cardiopulmonary Bypass
Lead Sponsor:
Antalya Training and Research Hospital
Conditions:
Intraocular Pressure
Anesthesia
Eligibility:
All Genders
18+ years
Brief Summary
The aim of the study to compare the effects of sevoflurane-based anesthesia and propofol-based total intravenous anesthesia on intraocular pressure (IOP) during coronary artery bypass graft surgery (C...
Detailed Description
Patients undergoing elective coronary artery bypass grafting surgery with cardiopulmonary bypass (CPB) were included in this prospective observational study. Patients with a history of cardiac surgery...
Eligibility Criteria
Inclusion
- Patients undergoing elective coronary artery bypass grafting surgery with cardiopulmonary bypass (CPB)
Exclusion
- history of cardiac surgery
- diabetic retinopathy
- cataract
- uncontrolled hypertension
- chronic kidney disease
- glaucoma
- previous eye surgery
- previous neurological disease
- allergy to propofol or sevoflurane
- baseline intraocular pressure (IOP) greater than 30 mmHg
Key Trial Info
Start Date :
September 1 2021
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
January 28 2022
Estimated Enrollment :
65 Patients enrolled
Trial Details
Trial ID
NCT06494969
Start Date
September 1 2021
End Date
January 28 2022
Last Update
July 10 2024
Active Locations (1)
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1
Health Science University, Antalya Training and Research Hospital
Antalya, Muratpasa, Turkey (Türkiye), 071**