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临床试验/CTRI/2026/01/100715
CTRI/2026/01/100715尚未招募4 期

COMPARATIVE STUDY OF SEVOFLURANE AND ISOFLURANE ON HEMODYNAMIC STABILITY ON PATIENTS UNDERGOING LAPAROSCOPIC SURGERY: A RANDOMIZED CLINICAL TRIAL

Regional Institute of Medical Sciences1 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2026年1月20日最近更新:

试验速览

阶段
4 期
状态
尚未招募
入组人数
84
试验地点
1

研究概览

简要总结

Laparoscopic surgeries have gained widespread acceptance across various surgical specialties due to their minimally invasive nature, reduced post operative pain, quicker recovery, and shorter hospital stays. Despite these advantages, laparoscopic procedures are associated with physiological alterations, including increased intraabdominal pressure and Carbon dioxide insufflation, which can pose significant challenges to maintaining hemodynamic stability during anesthesia. This becomes particularly important in patients safety and operative outcomes.

The present study is a prospective, randomized, and comparative clinical trial aimed at evaluating and comparing the effects of sevoflurane and isoflurane on intraoperative hemodynamic stability and post anesthesia recovery in patients undergoing various elective laparoscopic surgeries under general anesthesia.

A total of 84 patients, aged from 18 to 60 years and classified as ASA Grade I or II, scheduled for elective laparoscopic procedures, were enrolled in the study and randomly assigned into two equal groups

Group A    42 patients to receive sevoflurane for maintenance of anesthesia

Group B    42 patients to receive isoflurane for maintenance of anesthesia

All patients received standardized premedication and were induced with intravenous agents. Anesthesia was maintained with a mixture of oxygen and nitrous oxide , supplemented with either isoflurane or sevoflurane, titrated to maintain adequate depth of anesthesia by using MAC value and stable hemodynamic parameters.

Throughout the perioperative period, heart rate, systolic blood pressure, diastolic blood pressure, and mean arterial pressure were closely monitored. Postoperative recovery characteristics were also assessed, including

Time to eye opening

Response to verbal commands

Time to extubation

Modified aldrete score

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients of either sex Patients with ASA physical grade 1 and 2 Patients of age group 18 to 60 years.

排除标准

  • Difficult airway Uncontrolled Hypertension Uncontrolled Diabetes mellitus Ischemic heart disease Severe Renal disease Cerebrovascular disease Patients on beta blockers, alpha blockers Bronchial Asthma Allergy to study drugs.

研究者

申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Jiwanshu

Regional institute of medical sciences

研究点 (1)

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