Comparison of effects of inhalation anesthesia and total intravenous anesthesia in patients undergoing laparoscopic cholecystectomy

Comparison of effects of inhalation anesthesia and total intravenous anesthesia in patients undergoing laparoscopic cholecystectomy: a prospective, randomized, comparative clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0011502

Enrollment

Registered

2026-01-20

Start date

2025-12-17

Completion date

Unknown

Last updated

2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : Patients are randomly allocated by a computer-generated randomization table into two groups: sevoflurane (group S) and propofol (group P). After arrival in the operating room, standard monitori

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: i) Adults aged 20-64 years undergoing laparoscopic cholecystectomy ii) ASA (American Society of Anesthesiologists) physical status classification I-I)

Exclusion criteria

Exclusion criteria: 1) Patients with severe diseases classified as ASA class III or higher 2) Patients who have received sedatives, steroids, or opioid analgesics within 24 hours 3) Patients receiving psychiatric medications for mental disorders 4) Pregnant women or breastfeeding mothers 5) Patients with obesity (BMI > 30) or underweight (BMI < 20)

Design outcomes

Primary

Measure	Time frame
Quality of Recovery-15 (QoR-15) score for general anesthesia and postoperative recovery assessment	—

Secondary

Measure	Time frame
Postoperative pain intensity and analgesic requirements	—

Countries

Korea, Republic of

Contacts

Public ContactEun Kyung Choe

Yeongnam University Medical Center

zzini0527@naver.com+82-53-620-3361

Outcome results