The Effect of Intraoperative Magnesium Sulfate Infusion on the Postoperative Recovery

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

Status

Terminated

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03206008

Enrollment

Registered

2017-07-02

Start date

2016-11-18

Completion date

2017-11-24

Last updated

2018-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Brief summary

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

Interventions

DRUGMagnesium Sulfate

DRUGNormal saline

Placebo

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

SUPPORTIVE_CARE

Masking

TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Yes

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

Design outcomes

Primary

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

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026