Clinical Trials Directory

Trials / Completed

CompletedNCT01843296

Effects of Addition of Magnesium Sulfate in Spinal Anesthesia on Sensory-Motor Blocks and Postoperative Pain in Lumbar Disk Herniation Surgery

Comparison of the Effects of Three Methods of Intrathecal Bupivacaine; Bupivacaine-Fentanyl and Bupivacaine-Fentanyl-Magnesium Sulfate on Sensory-Motor Blocks and Postoperative Pain in Patients Undergoing Lumbar Disk Herniation Surgery

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
105 (actual)
Sponsor
Isfahan University of Medical Sciences · Academic / Other
Sex
All
Age
20 Years – 65 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to Compare three methods of intrathecal bupivacaine; bupivacaine-fentanyl; bupivacaine-fentanyl-magnesium sulfate on sensory-motor blocks and postoperative pain in patients undergoing lumbar disk herniation surgery.

Detailed description

* Comparison three methods of intrathecal bupivacaine;bupivacaine-fentanyl;bupivacaine-fentanyl-magnesium sulfate on sensory-motor blocks in patients undergoing lumbar disk herniation surgery * Comparison three methods of intrathecal bupivacaine;bupivacaine-fentanyl;bupivacaine-fentanyl-magnesium sulfate on postoperative pain in patients undergoing lumbar disk herniation surgery * Comparison three methods of intrathecal bupivacaine;bupivacaine-fentanyl;bupivacaine-fentanyl-magnesium sulfate on postoperative side effects in patients undergoing lumbar disk herniation surgery

Conditions

Interventions

TypeNameDescription
DRUGMagnesium SulfateInjection of 50 mg of magnesium sulfate 50% (0.1 ml),intrathecally.
PROCEDURESpinal AnesthesiaLumbar puncture was performed in sitting position,at the one level above iliac crest. Using a median approach, a 25-G Quincke needle was introduced with the needle aperture directed laterally.
DRUGBupivacaine
DRUGFentanyl

Timeline

Start date
2012-11-01
Primary completion
2012-12-01
Completion
2013-04-01
First posted
2013-04-30
Last updated
2013-07-02

Locations

1 site across 1 country: Iran

Source: ClinicalTrials.gov record NCT01843296. Inclusion in this directory is not an endorsement.