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Clinical Trials/NCT02011152
NCT02011152
Completed
Not Applicable

The Effect of Intravenous Magnesium Sulfate Infusion on Sensory Spinal Block and Postoperative Pain Score in Abdominal Hysterectomy

Karadeniz Technical University0 sites40 target enrollmentDecember 1998
ConditionsOperation

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Operation
Sponsor
Karadeniz Technical University
Enrollment
40
Primary Endpoint
pain scores
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The aim of this study was to investigate the effect of i.v. infusion of magnesium sulphate during spinal anesthesia on duration of spinal block and postoperative pain.

Registry
clinicaltrials.gov
Start Date
December 1998
End Date
December 1999
Last Updated
12 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Fatih Kahraman

The effect of intravenous magnesium sulfate infusion on sensory spinal block and postoperative pain score in abdominal hysterectomy

Karadeniz Technical University

Eligibility Criteria

Inclusion Criteria

  • ASA physical status I and II, aged between 18 and 65 female patients undergoing abdominal hysterectomy

Exclusion Criteria

  • severe cardiovascular, renal and hepatic dysfunction, neuromuscular diseases, using calcium channel blockers, and inappropriate for spinal anesthesia.

Outcomes

Primary Outcomes

pain scores

Time Frame: 6 mo

Secondary Outcomes

  • sensory block(6 mo)

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