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RECRUITING
NCT07662408
PHASE4

Comparison of Norepinehrine Versus Phenylepherine Infusion for Prevention of Post-spinal Hypotension

Sponsor: Sohag University

View on ClinicalTrials.gov

Summary

This prospective randomized double-blinded clinical trial aims to compare the efficacy and hemodynamic effects of prophylactic norepinephrine infusion versus phenylephrine infusion for prevention of spinal anesthesia-induced hypotension in elderly patients undergoing elective orthopedic hip surgery under subarachnoid block. Sixty-two patients aged 60 years or older will be randomly assigned into two equal groups to receive either norepinephrine infusion (8 µg/min) or phenylephrine infusion (100 µg/min) immediately after spinal anesthesia. The primary outcome is the mean heart rate during vasopressor infusion, while secondary outcomes include incidence of hypotension, severe hypotension, bradycardia, reactive hypertension, intraoperative fluid requirements, blood loss, transfusion requirements, and postoperative nausea and vomiting. Hemodynamic parameters will be monitored throughout surgery to evaluate the safety and effectiveness of both vasopressor strategies.

Official title: Comparison of Norepinephrine Versus Phenylephrine Infusion for Prevention of Hypotension Due to Subarachnoid Block in Elderly Patients Undergoing Orthopedic Hip Surgery:A Prospective Randomized Trial

Key Details

Gender

All

Age Range

60 Years - 100 Years

Study Type

INTERVENTIONAL

Enrollment

62

Start Date

2026-05-22

Completion Date

2027-03-14

Last Updated

2026-06-23

Healthy Volunteers

Yes

Interventions

DRUG

Norepinephrine

norepinephrine infusion at 8 µg/min. Infusion will continue for 45 minutes after spinal anesthesia.

DRUG

Phenylephrine

phenylephrine infusion at 100 µg/min. Infusion will continue for 45 minutes after spinal anesthesia.

Locations (1)

Sohag university hospital

Sohag, Egypt