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NOT YET RECRUITING
NCT07655596
PHASE4

Continuous Infusion Versus Intermittent IV Bolus of Cefazolin: Prevention of Surgical Site Infection During Orthopedic Surgeries in Egyptian Patients.

Sponsor: Helwan University

View on ClinicalTrials.gov

Summary

A randomozed control trial on adults who underwent orthopaedic surgery. To evaluate the effectiveness of intraoperative continuous infusion (CI) of cefazolin compared with intermittent (INT) cefazolin administration in preventing SSIs in the orthopaedic surgical population. Eligible patients will be randomized using block randomization into 2 groups: intervention group and control group. The intervention group will use continuous infusion of cefazolin (CI), while the control group will follow the traditional presurgical prophylaxis protocol of intermittent cefazolin doses (INT).

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-07-01

Completion Date

2026-12-31

Last Updated

2026-06-18

Healthy Volunteers

No

Interventions

DRUG

Cefazolin 2 g Infusion

Intraoperative continuous infusion (CI) of cefazolin

DRUG

Cefazolin 2 GM Injection

Administration of cefazolin 2 gm 30 minutes pre-surgery