Clinical Trial

Low-Flow Sevoflurane and Desflurane Anesthesia in Laparoscopic Cholecystectomy

Recruiting
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Summary
Several studies have demonstrated that inhalational anesthetic agents such as desflurane and sevoflurane may cause varying degrees of postoperative sore throat, hoarseness, and cough in orotracheally intubated patients. However, data evaluating these outcomes under low-flow anesthesia conditions remain limited and insufficient. This single-center, prospective, randomized controlled study will be conducted in patients aged 18-65 years, classified as American Society of Anesthesiologists (ASA) physical status I-II, who are scheduled to undergo elective laparoscopic cholecystectomy under general anesthesia and who provide written informed consent to participate in the study. The primary objective of the study is to compare the effects of low-flow desflurane and low-flow sevoflurane anesthesia on the incidence and severity of postoperative sore throat. The secondary outcomes include the evaluation of postoperative hoarseness and cough, the incidence of postoperative nausea and vomiting (PONV), and the total consumption of inhalational anesthetic agents.
Protocol Amendment History 1 change
critical Recruitment opened 2026-04-28
Trial Details
NCT Number NCT07440758
Lead Sponsor Kayseri City Hospital
Conditions Laparoscopic Cholecystectomy, Postoperative Sore Throat
Enrollment 70 participants
Start Date 2026-03-20
Primary Completion 2026-07-01 (estimated)
Study Completion 2026-07-30 (estimated)
Updated on ClinicalTrials.gov 2026-08-05