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Completed

NCT Number: NCT02011152

Spinal Anesthesia Magnesium Infusion

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.

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Key information

Conditions

Operation

Age range

18 year–65 year

Sex eligibility

Female

Study type

Observational

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. pain scores

    Time frame: 6 mo

Secondary outcomes

  1. sensory block

    Time frame: 6 mo

Other outcomes

  1. motor block

    Time frame: 6mo

Sponsors and collaborators

Lead sponsor

Karadeniz Technical University

Other

Registry information

Official study title

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

Important dates

Study start
1998
Primary completion
1999
Study completion
1999
First posted
Dec 13, 2013
Registry last updated
Dec 13, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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