Skip to content

The comparison of recovery profiles from the effects of two inhaled anaesthetic agents, Desflurane and Sevoflurane,in patients undergoing Laparoscopic Cholecystectomy

The Comparison of Recovery Profiles of Desflurane Versus Sevoflurane in Patients Undergoing Laparoscopic Cholecystectomy - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/12/010853
Enrollment
60
Registered
2017-12-12
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K802- Calculus of gallbladder without cholecystitis Health Condition 2: null- Patients undergoing Laparoscopic Cholecystectomy

Interventions

Intervention1: Desflurane: Inhaled Anaesthetic Agent PHYSICAL PROPERTIES Chemical name â?? 1,2,2,2-tetrafluoroethyl difluoromethyl Ether Molecular weight[g] â?? 168 Boiling Point [o C] - 24 Vapour pre

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1) ASA I and II patients. 2) Age group 20â??60 years. 3) Patients undergoing Laparoscopic Cholecystectomy

Exclusion criteria

Exclusion criteria: 1) Moderate to severe underlying Cardiopulmonary dysfunction. 2) Moderate to severe underlying Hepatic dysfunction. 3) Moderate to severe underlying Renal dysfunction. 4) Moderate to severe underlying Endocrine dysfunction. 5) Moderate to severe underlying Neurological dysfunction. 6) Pregnancy. 7) Psychiatric disorder. 8) History of drug allergy or abuse. 9) Documented allergic reaction to the anaesthetic agent being used. 10) Patients taking CNS depressants. 11) Patient refusal to participate in the study. 12) Intra operative conversion of procedure from laparoscopic to open.

Design outcomes

Primary

MeasureTime frame
1) To compare the time taken for awakening the patient after inhalational agent is switched off. 2) To compare the time taken for verbal response to occur after the inhalational agent is switched off. 3) To compare the time taken for complete recovery of patient as measured by a modified Aldrete score of â?¥ 9Timepoint: 1) At the time of administering Reversal 2) At the time of Extubation 3) 1 minute after extubation 4) 3 minutes after extubation 5) 5 minutes after extubation 6) 10 minutes after extubation 7) 15 minutes after extubation 8) 30 minutes after extubation 9) Time of switching off inhalational agent( to co incide with skin closure by the surgeon) 10) Time of first eye opening after switching off the agent 11) Time of first verbal response after switching off the agent

Secondary

MeasureTime frame
To document adverse effects, if any, during extubation or early recovery such as excessive secretions, coughing or laryngospasm.Timepoint: From switching off the inhalational agent, to complete awakening

Countries

India

Contacts

Public ContactDr Gauri Raman Gangakhedkar

P.D. Hinduja National Hospital and Medical Research Centre

monteiro04@gmail.com9821158949

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026