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Magnesium Sulfate; Postoperative Nausea and Vomiting; Laparoscopic Surgery

The Effect of Intravenous Magnesium Sulfate on Postoperative Nausea and Vomiting in Patients Undergoing Laparoscopic Gynecologic Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03541915
Enrollment
90
Registered
2018-05-31
Start date
2018-12-01
Completion date
2019-05-30
Last updated
2018-10-01

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

Conditions

Gynecologic Disease

Brief summary

Postoperative nausea and vomiting (PONV) is commonly accompanied in patients undergoing surgery under general anesthesia. The patients undergoing laparoscopic gynecologic surgery have multiple risk factors for developing PONV such as female gender, nonsmoker, postoperative opioids, and laparoscopic surgery. Thus, it is important to prevent PONV in these patients.

Detailed description

Magnesium is a N-methyl-D-aspartate (NMDA) antagonist that is known to be effective in reducing opioid consumption and controlling postoperative pain. This opioid reducing effect can be associated with reduction of the incidence of PONV. However, the effect of magnesium on preventing PONV have not been investigated before. Thus, the investigators hypothesized that intraoperative infusion of magnesium will be effective in preventing PONV in patients undergoing laparoscopic gynecologic surgery.

Interventions

20mg/kg of magnesium sulfate will be infused after induction of anesthesia. And magnesium sulfated will be continuously infused at a rate of 15mg/kg/h during the operation.

DRUGControl (saline)

The same volume of normal saline will be infused after induction of anesthesia and continuously infused at the same rate of magnesium.

Sponsors

Gangnam Severance Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Gynecologic disease * Female patients undergoing laparoscopic gynecologic surgery and receiving postoperative fentanyl based intravenous patient controlled analgesia (PCA), aged 20-65 years.

Exclusion criteria

* impaired renal or hepatic function (Glutamic Oxalacetate Transaminase \[GOT\]/Glutamic Pyruvate Transaminase \[GPT\]\>50, estimated glomerular filtration rate \[eGFR\]\<60) * atrioventricular block, myopathies, diabetes, treated with calcium channel blockers * History of receiving antiemetics within 1 day before surgery * History of receiving opioids or non-steroidal anti-inflammatory drugs within 1 week of surgery * drugs or alcohol abuse * patients treated with isoniazid, chlorpromazine, or digoxin * patients who cannot communicated with others or with cognitive dysfunction * patients who cannot read informed consent

Design outcomes

Primary

MeasureTime frameDescription
The incidence of PONVup to postoperative 2 daysThe incidence of PONV will be measured up to postoperative 2 days.

Outcome results

None listed

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