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A clinical trail to study the effect of two drugs desflurane and sevoflurane in adults after laparoscopic surgery.

A randomized controlled comparison of emergence agitation and recovery profile between desflurane and sevoflurane anaesthesia in adults after laparoscopic surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/03/012473
Enrollment
60
Registered
2018-03-12
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: null- patients undergoing laparoscopic surgery under general anaesthesia

Interventions

Intervention1: desflurane: inhalational anaesthetic agent Control Intervention1: sevoflurane: inhalational anaesthetic agent

Sponsors

Director Principal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age group between 18 and 60 years. 2. American Society of Anaesthesiologist (ASA) physical status I and II 3. Patients scheduled for elective laparoscopy surgery under general anaesthesia with duration of surgery less than 90 minutes.

Exclusion criteria

Exclusion criteria: 1. Patients with clinically significant cardiovascular, respiratory, hepato-renal, endocrine or metabolic disorders. 2. Patients with gastro-esophageal reflux disease. 3. Patients with neuropsychiatric disorders. 4. Patients with mental retardation. 5. Patients with a body mass index (BMI) > 35 kg.m.-2 6. Patients taking any central nervous system depressants. 7. Patients on chronic opioids, corticosteroids or any sleep aid drugs. 8. Patients having alcohol or any drug abuse. 9. Patients with any allergy to study drugs. 10.Pregnant and breastfeeding patients.

Design outcomes

Primary

MeasureTime frame
Severity of emergence agitation by Aonos Four point ScaleTimepoint: 1.Immediately after the PLMA is removed in the Operating Room. 2.At admission in PACU. 3.Thereafter every 10 minutes in the recovery period, till the patient is discharged from PACU.

Secondary

MeasureTime frame
Any perioperative complicationsTimepoint: Perioperative period;Heart RateTimepoint: 1.Prior to induction 2.Ten minutes after induction. 3.After PLMA removal. 4.At admission in PACU. 5.Immediately Prior to discharge from PACU.;Mean Arterial PressureTimepoint: 1.Prior to induction 2.Ten minutes after induction. 3.After PLMA removal. 4.At admission in PACU. 5.Immediately Prior to discharge from PACU;Non Invasive Blood PressureTimepoint: 1.Prior to induction 2.Ten minutes after induction. 3.After PLMA removal. 4.At admission in PACU. 5.Immediately Prior to discharge from PACU;Quality of Recovery by QOR-40 score.Timepoint: 1.The day before surgery (baseline) 2.Postoperative day one (POD1,around 24 hours after surgery) 3.Postoperative day two (POD2, around 48 hours after surgery).;Saturation of Oxygen in Blood.Timepoint: 1.Prior to induction 2.Ten minutes after induction. 3.After PLMA removal. 4.At admission in PACU. 5.Immediately Prior to discharge from PACU.;Severity of anxiety using an 11-point numeric rating score (NRS)Timepoint: 1.In Preoperative room. 2.Immediately upon arrival in the PACU 3.Thereafter every 10 minutes in the recovery period, till the patient is discharged from PACU.;Severity of nausea/vomiting using an 11-point numeric rating score (NRS)Timepoint: 1.In Preoperative room. 2.Immediately upon arrival in the PACU 3.Thereafter every 10 minutes in the recovery period, till the patient is discharged from PACU.;Severity of pain using an 11-point numeric rating score (NRS)Timepoint: 1.In Preoperative room. 2.Immediately upon arrival in the PACU 3.Thereafter every 10 minutes in the recovery period, till the patient is discharged from PACU.

Countries

India

Contacts

Public ContactDheeraj Kapoor

Government medical college and hospital, Chandigarh

kapoor.dheeraj72@gmail.com9646121549

Outcome results

None listed

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