NCT06889090View on ClinicalTrials.gov

Comparing Effect of Opioid-sparing Versus Conventional Anesthesia on Quality of Recovery After Emergency Laparotomy

NANot yet recruitingINTERVENTIONAL
Enrollment

120

Participants

Timeline

Start Date

April 20, 2025

Primary Completion Date

April 30, 2026

Study Completion Date

May 12, 2026

Conditions
Anesthesia Recovery Period
Interventions
DRUG

: two syringes of lidocaine 10 mg/mL will be prepared. A 10-mL syringe (induction syringe) will be given during the induction of anesthesia and A 50 mL syringe (infusion syringe) will be used as conti

: two syringes of lidocaine 10 mg/mL will be prepared. A 10-mL syringe (induction syringe) will be given during the induction of anesthesia and A 50 mL syringe (infusion syringe) will be used as continuous infusion.

DRUG

A 10-mL syringe of 10 mcg/mL fentanyl (induction syringe) and a 50-mL syringe of saline (infusion syringe) will be prepared as placebo.

A 10-mL syringe of 10 mcg/mL fentanyl (induction syringe) and a 50-mL syringe of saline (infusion syringe) will be prepared as placebo.

All Listed Sponsors
lead

Cairo University

OTHER

NCT06889090 - Comparing Effect of Opioid-sparing Versus Conventional Anesthesia on Quality of Recovery After Emergency Laparotomy | Biotech Hunter | Biotech Hunter