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Valproic Acid, Magnesium Sulphate, Rocuronium Requirement, Postoperative Analgesia

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Seoul National University

Status

Unknown

Conditions

Cerebral Aneurysm

Treatments

Drug: Magnesium Sulfate
Drug: 0.9% saline

Study type

Interventional

Funder types

Other

Identifiers

NCT01460563
Mg_orfil

Details and patient eligibility

About

The investigators hypothesized that valproic acid will increase rocuronium requirement and MgSO4 infusion would reduce requirement of muscle relaxant in craniotomy patients preloaded with sodium valproate.

Full description

Magnesium sulfate (MgSO4) is known to reduce requirement of muscle relaxant.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18- 65 years
  • American society of anesthesiology physical status 1,2
  • scheduled for elective craniotomy for aneurysm clipping or for superficial temporal artery-middle cerebral artery anastomosis

Exclusion criteria

body mass index <18.5 or >24.9 kg m-2; neuromuscular, renal, cardiovascular or hepatic insufficiency; Glasgow coma scale (GCS) <15; allergy to the study drugs; medications influencing NDMRs; breast feeding; pregnancy; and preoperative epilepsy.

Trial design

60 participants in 3 patient groups, including a placebo group

Mg_orfil
Experimental group
Description:
patients preloaded with sodium valproate receives MgSO4 during the craniotomy.
Treatment:
Drug: Magnesium Sulfate
control_orfil
Placebo Comparator group
Description:
patients preloaded with sodium valproate receives 0.9% saline as placebo.
Treatment:
Drug: 0.9% saline
Drug: 0.9% saline
control_no orfil
Placebo Comparator group
Description:
patients not preloaded with sodium valproate receives 0.9% saline as placebo.
Treatment:
Drug: 0.9% saline
Drug: 0.9% saline

Trial contacts and locations

1

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Central trial contact

Mihyun Kim, Doctor

Data sourced from clinicaltrials.gov

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