Comparison of 3 doses of anesthetic for spinal anesthesia in cesarean sectio

Phase 2

Recruiting

• Conditions: Cesarean delivery.; Newborn (suspected to be) affected by Cesarean delivery; P03.4

• Registration Number: IRCT20130812014333N156
• Lead Sponsor: Kermanshah University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 5 January 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 108

Inclusion Criteria

Cesarean section patients between 18 and 42 years old
Weight between 60 to 90 kg
Height between 155 and 175
Gestational age equal or greater than 36 weeks

Exclusion Criteria

History of coagulation problems
Increased intracranial pressure
Local anesthetic allergy
Infection at the site of needle entry

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Patient satisfaction with spinal anesthesia. Timepoint: After surgery. Method of measurement: Question from the patient (excellent, good, average, bad).;Blood pressure. Timepoint: Every 3 minutes from the start of the block until the recovery clearance. Method of measurement: Monitoring device.;Heart rate. Timepoint: Every 3 minutes from the start of the block until the recovery clearance. Method of measurement: Monitoring device.