Propofol Versus Sevoflurane Anesthesia on the Intraocular Pressure and Hemodynamics in Patient Undergoing Cyclophotocoagulation
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Propofol and Fentanyl administration, Sevoflurane and fentanyl administration.
- Who it may be relevant to
- Registry conditions: Patient Cataract. Basic parameters: 15 years — 50 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Comparative Study Between the Effects of Propofol Versus Sevoflurane Anesthesia on the Intraocular Pressure and Hemodynamics in Patient Undergoing Cyclophotocoagulation (Cpc )Operation
Overview
we use two different technique of anaesthesia for anaesthesia of patient undergoining CPC operation (20 each) were comparable with regard to demographic data and hemodynamic variables, IOP. After approval by our local Ethics Committee and written informed consent, 40 ASA physical status I, II or III patients scheduled for elective CBC operations were included in this study group s anasthetized with sevofluran while group p anaesthetized with propofol with repeated measurment of intraocular pressure of the other eye to detect which method better for IOP.
Interventions
- Drug Propofol and Fentanyl administration
Group P patient anaesthetized by propofol and fentanyle for induction and maintenance - Drug Sevoflurane and fentanyl administration
Group S patient anaesthetized by sevoflurane and fentanyl for induction and maintenance
Primary outcome measures
- measurement of Intra ocular pressure during different type of anesthesia [Time frame: 2 minute after administration of muscle relaxant and every 5 minute until termination of surgery]
Eligibility criteria
Inclusion criteria
ASA I to III
Exclusion criteria
- known allergies; adverse reactions to any of the anesthetic agents used in the study
- unstable angina or manifest congestive heart failure.
- airway management was expected to be difficult
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Supportive care
Study locations
Egypt · 1 center
- Suhag faculty of medicine — Sohag
Identifiers
NCT: NCT07445672 · soh-med-25-9----2PD