Recovery and perioperative outcomes of propofol-based anesthesia versus sevoflurane for ERCP: a randomized clinical trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR202608489781500

Enrollment

Registered

2026-08-13

Start date

2022-08-01

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

Anaesthesia

Interventions

propofol based TIVA

Sevoflurane anesthesia

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Adults aged 18–65 years American Society of Anesthesiologists (ASA) physical status I–III Scheduled for elective endoscopic retrograde cholangiopancreatography (ERCP) under general anesthesia Provided written informed consent

Exclusion criteria

Exclusion criteria: Emergency ERCP Refusal to provide informed consent Morbid obesity Hepatic encephalopathy Coagulation abnormalities Allergy to study drugs or contrast agents Significant behavioral disorders

Design outcomes

Primary

Measure	Time frame
Time to spontaneous eye opening Time to response to verbal commands Time to adequate muscle power Time to extubation	—

Secondary

Measure	Time frame
Intraoperative hemodynamic variables Postoperative complications Patient satisfaction Postoperative pain score	—

Countries

Nigeria

Contacts

Public ContactOlusegun Alatise

Head of Dept of Surgery

segunalatishe@yahoo.co.uk2348033859387

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026