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NCT03206008 Clinical Trial

The Effect of Intraoperative Magnesium Sulfate Infusion on the Postoperative Recovery

Postoperative Pain Clinical Trial

Official title:
The Effect of Intraoperative Magnesium Sulfate Infusion on the Postoperative Recovery After Outpatient Surgery

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT03206008
Other study ID # B-1608-360-006
Secondary ID
Status Terminated
Phase N/A
First received June 30, 2017
Last updated April 19, 2018
Start date November 18, 2016
Est. completion date November 24, 2017

Study information
Verified date April 2018
Source Seoul National University Bundang Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluating analgesic effect of intraoperative magnesium sulfate infusion in the outpatient surgery case

Recruitment information / eligibility
Status Terminated
Enrollment 11
Est. completion date November 24, 2017
Est. primary completion date November 24, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- aged between 18-65 year-old-patient (ASA I-II) who are planned to undergoing day surgery

Exclusion Criteria:

- ASA class = III

- suspected imbalance of electrolyte

- myocardial damage or conduction delay

- myasthenia gravis or other neuromuscular disease

- impaired renal function

- already using any type of analgesia

- denial of participating in the study or not giving the informed consent

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Magnesium Sulfate

• Normal saline
Placebo

Locations
Country Name City State
Korea, Republic of Seoul National University Bundang Hospital, department of Anesthesia and pain Seongnam Gyenggo-do

Sponsors (1)
Lead Sponsor Collaborator
Seoul National University Bundang Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary severity of postoperative pain checking the postoperative pain in score at the recovery room and outpatient surgery center 1 hour interval
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