NCT02011152

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.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Dec 1998

Shorter than P25 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 1998

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 1999

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 1999

Completed
14 years until next milestone

First Submitted

Initial submission to the registry

December 10, 2013

Completed
3 days until next milestone

First Posted

Study publicly available on registry

December 13, 2013

Completed
Last Updated

December 13, 2013

Status Verified

December 1, 2013

Enrollment Period

1 year

First QC Date

December 10, 2013

Last Update Submit

December 12, 2013

Conditions

Operation

Outcome Measures

Primary Outcomes (1)

  • pain scores

    6 mo

Secondary Outcomes (1)

  • sensory block

    6 mo

Other Outcomes (1)

  • motor block

    6mo

Eligibility Criteria

Age18 Years - 65 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

18 and 65 female patients undergoing abdominal hysterectomy

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Fatih Kahraman

    KTU

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Target Duration
3 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
The effect of intravenous magnesium sulfate infusion on sensory spinal block and postoperative pain score in abdominal hysterectomy

Study Record Dates

First Submitted

December 10, 2013

First Posted

December 13, 2013

Study Start

December 1, 1998

Primary Completion

December 1, 1999

Study Completion

December 1, 1999

Last Updated

December 13, 2013

Record last verified: 2013-12