Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
COMPLETED
NCT07838909
NA

Intraoperative Ketamine Versus Lidocaine Infusion on Postoperative Cognitive Dysfunction in Patients Undergoing Hip Surgery

Sponsor: Tanta University

View on ClinicalTrials.gov

Summary

This study aims to compare effects of ketamine versus lidocaine on postoperative cognitive dysfunction in geriatric patient undergoing hip surgery.

Official title: Effect of Intraoperative Ketamine Versus Lidocaine Infusion on Postoperative Cognitive Dysfunction in Elderly Patients Undergoing Hip Surgery

Key Details

Gender

All

Age Range

66 Years - Any

Study Type

INTERVENTIONAL

Enrollment

120

Start Date

2025-03-30

Completion Date

2026-03-30

Last Updated

2026-09-24

Healthy Volunteers

No

Interventions

DRUG

Group Ketamine

Patients will receive ketamine as a bolus (0.5 mg/kg) after induction of spinal anesthesia, followed by a continuous infusion (0.2 mg/kg. h) until the end of surgery.

DRUG

Group Lidocaine

Patients will receive lidocaine as a bolus (1.5 mg/kg) after induction of spinal anesthesia, followed by a continuous infusion (2 mg/kg. h) until the end of surgery

DRUG

Group Placebo

Patients will receive placebo (saline) and administered in equal volumes and in the same manner as a control group.

Locations (1)

Tanta University

Tanta, Egypt