Spinal Anesthesia Magnesium Infusion

Operation Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02011152
• Other study ID #: 199812
• Secondary ID: spinal magnesium
• Status: Completed
• Phase: N/A
• First received: December 10, 2013
• Last updated: December 12, 2013
• Start date: December 1998
• Est. completion date: December 1999

Study information

• Verified date: December 2013
• Source: Karadeniz Technical University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Turkey: Ministry of Health
• Study type: Observational [Patient Registry]

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: December 1999
• Est. primary completion date: December 1999
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 65 Years

Eligibility

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.

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

• Operation

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Karadeniz Technical University

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	motor block		6mo	No
Primary	pain scores		6 mo	Yes
Secondary	sensory block		6 mo	No