drugset / Trial / NCT07259655

Management of Post-Induction Hypotension in Emergency Abdominal Surgery

NCT07259655

Phase 4 Terminated 100 enrolled Hopital Charles Nicolle
RandomizedParallel-groupTriple-blindTreatment

Summary

The goal of this clinical trial is to compare the efficacy of two vasopressors (norepinephrine vs. ephedrine) in treating hypotension in adult patients (aged 18+, ASA I-III) undergoing general anesthesia for abdominal surgical emergencies (e.g., appendicitis, intestinal obstruction, peritonitis). The main questions it aims to answer are: * Which drug is more effective at maintaining intraoperative blood pressure (SBP ≥ 80% of baseline)? * How many boluses of each vasopressor are required to maintain target blood pressure? Researchers will compare the norepinephrine group (receiving 10 µg boluses) to the ephedrine group (receiving 6 mg boluses) to see if norepinephrine is superior for maintaining hemodynamic stability and reduces the number of interventions needed. Participants will: * Be randomly assigned to receive one of the two study drugs. * Undergo standard general anesthesia with close hemodynamic monitoring. * Receive boluses of the assigned vasopressor whenever their blood pressure drops below a predefined threshold.

Timeline

Start
2025-03-06
Primary completion
2025-05-06
Completion
2025-05-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ephedrine Small molecule 6 mg Intravenous
Comparator Norepinephrine Other / unclassified 10 ug Intravenous

Indications