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Study identifier: NCT07440758 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Low-Flow Sevoflurane and Desflurane Anesthesia in Laparoscopic Cholecystectomy

Condition: Laparoscopic Cholecystectomy · Postoperative Sore Throat  ·  Sponsor: Kayseri City Hospital

PhaseNA
Planned participants70
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Emine Sümeyye Akköze  ·  +903523157700  ·  smyyclk51@gmail.com

Şaziye Burcu Tufaoğulları Erdoğan  ·  +903523157700  ·  burcutuf@yahoo.com

Always discuss trial participation with your own doctor first.

Locations (1)

Kayseri City HospitalKayseri, Kocasinan, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07440758