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A Study to compare the effects on induction , maintenance and recovery in general anaesthesia using propofol and sevoflurane respectively in adult patients

Comparative Study Of Effects Of Sevoflurane And Propofol During Induction ,Maintenance And Recovery Of General Anaesthesia In Adults:A Prospective Randomised Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/08/044983
Enrollment
168
Registered
2022-08-26
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: K807- Calculus of gallbladder and bile duct without cholecystitis

Interventions

Intervention1: Effects of Propofol during induction maintenance and recovery from general anaesthesia in adult patients: Propofol is given in iv route then iTime to loss of verbal response or apnoe

Sponsors

Department of Anaesthesiology IPGMER And Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients providing informed written consent Patients belonging to classs ASA 1 And ASA 2 Patients undergoing elective surgeries for chronic calculous diseases of gall bladder and biliary tract with operative duration of 2 to 3 hours

Exclusion criteria

Exclusion criteria: Patient refusal to participate Patients belonging to ASA 3 and ASA 4 Patient having known allergy to anaesthetic drugs involved in study Patients on medications like hypnotics narcotic analgesics or sedatives Patients having sensory or motor deficit Patients having hypotension or vascular disease History of seizure disorder Presence or History of anticipated difficult airway

Design outcomes

Primary

MeasureTime frame
Comparison of induction of the two anaesthetic agents with respect to time to loss of consciousness , requirement of analgesics and muscle relaxants , post operative nausea vomiting , emergence and post operative level of sedationTimepoint: End of surgery

Secondary

MeasureTime frame
Comparison of hemodynamic parameters of the patients between the two anaesthetic agentsTimepoint: intraoperative time period

Countries

India

Contacts

Public ContactDr Arpita Laha

IPGMER And SSKM Hospital

arpita_laha@yahoo.com9433326667

Outcome results

None listed

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