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Spinal Anesthesia Magnesium Infusion

NCT ID: NCT02011152

Last Updated: 2013-12-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

1998-12-31

Study Completion Date

1999-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Operation

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Karadeniz Technical University

OTHER

Sponsor Role lead

Responsible Party

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Fatih Kahraman

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

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Fatih Kahraman

Role: PRINCIPAL_INVESTIGATOR

KTU

Other Identifiers

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spinal magnesium

Identifier Type: OTHER

Identifier Source: secondary_id

199812

Identifier Type: -

Identifier Source: org_study_id