Clinical Trials Directory

Trials / Completed

CompletedNCT07421817

Dexamethasone for Prevention of Postoperative Vomiting After Laparoscopic Gynecologic Surgery

Effect of a Preoperative Single Dose of Intravenous Dexamethasone on Postoperative Vomiting in Patients Undergoing Laparoscopic Gynecologic Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Rawalpindi Medical College · Academic / Other
Sex
Female
Age
15 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Postoperative nausea and vomiting (PONV) are common and distressing complications following laparoscopic gynecologic surgery. This randomized controlled trial evaluated whether a single preoperative intravenous dose of dexamethasone reduces postoperative vomiting compared with placebo and explored patient-related risk factors associated with PONV. Women undergoing elective laparoscopic gynecologic surgery were randomly assigned to receive dexamethasone (5 mg IV) or placebo at induction of anesthesia. The primary outcome was the incidence of postoperative vomiting within 24 hours, with secondary outcomes including nausea severity, rescue antiemetic use, and postoperative recovery parameters.

Detailed description

This single-blind randomized controlled trial evaluated the prophylactic efficacy of a single preoperative intravenous dose of dexamethasone for preventing postoperative vomiting in women undergoing elective laparoscopic gynecologic surgery. The study was conducted at Holy Family Hospital, Rawalpindi Medical University, Pakistan, between October 1, 2017, and March 31, 2018. Eligible women aged 15-65 years were randomized in a 1:1 ratio to receive either dexamethasone 5 mg intravenously or placebo (normal saline) at induction of anesthesia. Perioperative anesthesia and postoperative care were standardized across groups. The primary outcome was the incidence of postoperative vomiting within 24 hours after surgery. Secondary outcomes included nausea severity, need for rescue antiemetics, postoperative opioid use, and recovery parameters such as time to oral intake and mobilization. An exploratory analysis assessed patient-related predictors of postoperative nausea and vomiting, including body mass index and prior history of PONV.

Conditions

Interventions

TypeNameDescription
DRUGDexamethasoneSingle intravenous dose of dexamethasone 5 mg administered at induction of anesthesia prior to surgical incision.
OTHERPlacebo (Normal Saline)Single intravenous dose of 2 mL normal saline (placebo) administered at induction of anesthesia immediately prior to surgical incision, matched in volume to the dexamethasone administered in the experimental arm.

Timeline

Start date
2017-10-01
Primary completion
2018-03-31
Completion
2018-03-31
First posted
2026-02-19
Last updated
2026-02-20

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT07421817. Inclusion in this directory is not an endorsement.