intravenous bolous of Nor epinephrine and Ephedrine in prevention of post spinal hypotension in cesarean sectio

Phase 1

Recruiting

• Conditions: Spinal anesthesia in cesarean section.; Single liveborn infant, delivered by cesarean; Z38.01

• Registration Number: IRCT20120915010841N17
• Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 August 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 100

Inclusion Criteria

Satisfaction to participate in the project
Pregnant women aged 18 to 46
Pregnant women who underwent cesarean section under spinal anesthesia

Exclusion Criteria

sensitivity to medications used
Patients who have failed spinal anesthesia and undergo general anesthesia
Lung disease, heart disease, asthma, fever, hypertension, preeclampsia and eclampsia, cardiac arrhythmia

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hypotension. Timepoint: Every two minutes to 10 minutes, then every 5 minutes to 15 minutes, then every 10 minutes until the end of the surgery. Method of measurement: Non-invasive blood pressure.

Secondary Outcome Measures

Name	Time	Method
ausea & vomiting. Timepoint: after delivery. Method of measurement: Observation.;New born Apgar. Timepoint: 1&5 minutes after delivery. Method of measurement: Apgar Score.;Headache. Timepoint: after delivery. Method of measurement: Observation.