Evaluation of analgesic efficacy of lidocaine infusion in cesarean sectio

Not Applicable

• Conditions: Cesarean section.; Delivery by caesarean section, unspecified

• Registration Number: IRCT201610023051N11
• Lead Sponsor: Vice Chancellor for research of Qazvin University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 80

Inclusion Criteria

Inclusion criteria : Elective cesarean surgery; patients aged 18 to 45 years, ASA class 1 and 2.
Exclusion criteria: complete heart block; Severe bleeding and coagulation disorder; Severe hypotension and shock; septicemia; history of CNS disease; hyperthyroidism; hypertension; history of hepatorenal disease; Cardiovascular disease; diabetes; Allergy to lidocaine; placenta praevia; Placental abruption; cesarean induced deceleration Fetal heart rate (FHR); meconium; addict; contradiction of regional analgesia; eclampsia and preeclampsia; user of Beta blocker and glycoside.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time to first analgesic requirement. Timepoint: During 24 hrs after the surgery. Method of measurement: Hour.;Sensory block level and recovery of sensory block to T10. Timepoint: 30 and 60 seconds after injection. Method of measurement: Pin prick method.;Motor block level and recovery of motor block. Timepoint: 30 and 60 seconds after injection. Method of measurement: Bromage scale.;Hemodynamic changes (bradycardia, hypotension and Oxygen saturation <90] ). Timepoint: From the time of intervention; every 5 minute until 15 minute then every 15 minute until 1 hour. Method of measurement: Monitoring devise.

Secondary Outcome Measures

Name	Time	Method
Secondary effects. Timepoint: During 6 hrs after the surgery. Method of measurement: According patient's history.;Neonate APGAR. Timepoint: In the first and fifth minute from birth. Method of measurement: APGAR criteria.