Comparison of the effect of adding Neostigmine to Ropivacaine and sufentanilto Ropivacaine in spinal anesthesia for herniorrhaphy surgery

Phase 2

Recruiting

• Conditions: Spinal anesthesia.; Intentional self-poisoning by and exposure to other and unspecified drugs, medicaments and biological substances

• Registration Number: IRCT20141209020258N107
• Lead Sponsor: Arak University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 May 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 105

Inclusion Criteria

18 to 60 years
Patients candidate inguinal hernia surgery
Lack of cardiovascular problems
Absence of coagulation disorders
Lack of peripheral and central neuropathy
No history of allergy to Neostigmine and Ropivacaine and Sufentanil
Non-localized infection in the spinal cord

Exclusion Criteria

Patient dissatisfaction
Failure to perform spinal anesthesia

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Mean arterial blood pressure. Timepoint: Every 15 minutes during surgery and recovery time and up to 2 hours after surgery. Method of measurement: Barometer.;Heart rate. Timepoint: Every 15 minutes during surgery and recovery time and up to 2 hours after surgery. Method of measurement: Count.;Percent of oxygen saturation. Timepoint: Every 15 minutes during surgery and recovery time and up to 2 hours after surgery. Method of measurement: Pulse oximetry.;Duration of motor block. Timepoint: Every 5 minute. Method of measurement: Minute.;Duration of Sensory block. Timepoint: Every 1minute. Method of measurement: Minute.;Pain. Timepoint: Recovery and 2, 4, 8, 12 and 24 hours after surgery. Method of measurement: Visual Analogue Scale Questionnaire.;Mean of narcotic. Timepoint: 24 hour after surgery. Method of measurement: Milligram.