Actively Recruiting
Comparing Two Doses of Norepinephrine Bolus to Treat Low Blood Pressure During Emergency Abdominal Surgery
Led by Cairo University · Updated on 2026-08-05
136
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
The trial investigates the treatment of postinduction hypotension, a common complication during emergency abdominal surgery caused by factors like sepsis and low blood volume. This condition can lead to serious organ damage, so preventing and managing it quickly is important. The study compares two doses of norepinephrine bolus5 mcg and 10 mcgto find the best approach for treating low blood pressure in this setting. Participants will be randomly assigned to receive either a 5 mcg or 10 mcg norepinephrine bolus if their mean arterial pressure drops below 65 mmHg during surgery. The drug is prepared by diluting norepinephrine to a concentration of 10 mcgmL, then further diluted for dosing. If blood pressure does not improve within 2 minutes, the bolus may be repeated up to three times, followed by an infusion if needed. Fluid status will be assessed using leg raising maneuvers and fluid boluses before surgery, and heart rate and blood pressure will be monitored every 2 minutes for 30 minutes after skin incision. During the study, participants will undergo close blood pressure and heart rate monitoring at specified intervals. Researchers will measure the success of managing hypotension from anesthesia induction until 30 minutes after surgery begins. They will also assess the time and extent of low blood pressure, episodes of slow heart rate, and high blood pressure. The entire participation period covers the time from anesthesia induction to 30 minutes post-incision, focusing on immediate treatment response and safety under surgical conditions.
CONDITIONS
Brief Title
5 Versus 10 mcg Norepinephrine Bolus in Treatment of Postinduction and Early Intraoperative Hypotension in Emergency Abdominal Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients aged 21 to 65 years
- American Society of Anesthesiologists (ASA) physical status I to III
- Undergoing emergency abdominal surgery
You will not qualify if you...
- Severe heart conditions such as impaired contractility with ejection fraction less than 45%, heart block, arrhythmias, or severe valve disease
- Currently receiving vasopressor infusion
- Pregnant or lactating women
- Allergy to any of the study drugs
Research Team
M
Maha Mostafa, MD
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