Comparison of 10 and 12 mg doses of intrathecal bupivacaine %0.5 on sensory block level and postdural puncture headache in patients under repeated spinal

Phase 2

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

• Registration Number: IRCT20120915010841N20
• 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: 7 October 2019

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 40

Inclusion Criteria

Patient's consent to participate in the study
No history for diabetes, high blood pressure, heart disease
Patients who have failed spinal anesthesia and undergo general anesthesia

Exclusion Criteria

Patients with contraindications of spinal anesthesia (ICP increase, shock, history of coagulation problems ..)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Quality motor block. Timepoint: 5-10-15 and30 minutes after analgesia. Method of measurement: Bromage scure.;Sensory block quality. Timepoint: 5-10-15 and30 minutes after analgesia. Method of measurement: visual analgesic scale.;Headache. Timepoint: A week after surgery. Method of measurement: visual analgesic scale.

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.