COMPARISON BETWEEN EFFICACY OF NOREPINEPHRINE AND PHENYLEPHRINE BOLUSES FOR PREVENTION OF SPINAL ANAESTHESIA INDUCED HYPOTENSION IN OBSTETRICAL PATIENTS UNDERGOING EMERGENCY CESAREAN SECTION- A Double Blind Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to learn if norepinephrine is more effective than phenylephrine for prevention of spinal anesthesia induced hypotension. The main questions it aims to answer are: Does norepinephrine lower the incidence of spinal anesthesia induced hypotension in emergency obstetrical patients? We will compare effectiveness of norepinephrine and phenylephrine for the prevention of spinal anesthesia induced hypotension. Participants will: Be administered prophylactic boluses of both drugs right after spinal anesthesia induction and maternal hemodynamic parameters and neonatal APGAR scores will be recorded

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 40
Healthy Volunteers: f
View:

• American society of anesthesiologists II and III patients

• Age 18-40years

• Gestational age 32 weeks and above

Locations
Other Locations
Pakistan
Dr Ruth km pfau civil hospital karachi Dow University of health sciences, department of anesthesiology
RECRUITING
Karachi
Contact Information
Primary
Rabia Kamal, MBBS
rabiakamal.ae@gmail.com
923342239607
Backup
Arsalan Jamil, FCPS
22arsalan@gmail.com
923341226693
Time Frame
Start Date: 2024-12-31
Estimated Completion Date: 2025-03-31
Participants
Target number of participants: 124
Treatments
Active_comparator: Group P
Prophylactic bolus of phenylephrine will be administered right after spinal anesthesia induction
Experimental: Group N
Prophylactic bolus of norepinephrine will be administered right after spinal anesthesia.
Related Therapeutic Areas
Sponsors
Leads: Dow University of Health Sciences

This content was sourced from clinicaltrials.gov