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COMPLETED
NCT07651150
NA

DEX-HIP Trial: Preoperative IV Dexamethasone 4 mg vs Placebo to Reduce Postoperative Delirium Burden in Adults ≥70 Undergoing Hip Fracture Surgery

Sponsor: Jinnah Postgraduate Medical Centre

View on ClinicalTrials.gov

Summary

This single-center, prospective, randomized, double-blind, placebo-controlled trial was conducted at the Department of Orthopaedic Surgery, JPMC, Karachi. Patients aged ≥60 years with hip fractures were randomized 1:1 to receive either intravenous dexamethasone or a placebo preoperatively. The primary outcome was the incidence of POD within the first five postoperative days or until discharge, assessed via the Confusion Assessment Method. Delirium severity was quantified using the validated Memorial Delirium Assessment Scale.

Official title: DEX-HIP Trial: Preoperative IV Dexamethasone 4 mg vs Placebo to Reduce Postoperative Delirium Burden in Adults ≥70 Undergoing Hip Fracture Surgery : a Randomized Double-blind Trial.

Key Details

Gender

All

Age Range

60 Years - Any

Study Type

INTERVENTIONAL

Enrollment

120

Start Date

2026-01-01

Completion Date

2026-04-15

Last Updated

2026-06-16

Healthy Volunteers

No

Interventions

DRUG

Dexamethasone

A single 4 mg intravenous dose administered preoperatively.

DRUG

Placebo

Participants received an equivalent volume of normal saline placebo preoperatively.

Locations (1)

JPMC Karachi

Karachi, Sindh, Pakistan