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Effect of Intravenous Dextrose on PONV in Patients Undergoing Gynecological Laparoscopy

W

Weifang Medical University

Status

Enrolling

Conditions

Postoperative Nausea and Vomiting

Treatments

Other: lactated ringers
Other: 5% glucose

Study type

Interventional

Funder types

Other

Identifiers

NCT05932160
2023YX104

Details and patient eligibility

About

This study is to explore the relationship between intravenous infusion of dextrose during emergence from anesthesia and the incidence of PONV in patients undergoing gynecology laparoscopy (GL).

Enrollment

108 estimated patients

Sex

Female

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. ASA I or II;
  2. Performing gynecologic laparoscopic procedures under general anesthesia;

Exclusion criteria

  1. age <18 or >75
  2. severe hypertension,diabetes mellitus, significant hepatic or renal disease
  3. inability to follow protocol
  4. refusal to participant

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

108 participants in 2 patient groups

Experimental group
Active Comparator group
Description:
Patients in the experimental group were infused intravenously with 5% dextrose (400 ml/h) in the PACU. The study outcomes were collected at three assessment periods, 0-0.5 h, 0.5-6 h, 6-24 h, after anesthesia by an independent investigator.
Treatment:
Other: 5% glucose
Control group
Active Comparator group
Description:
Patients in the control group were infused intravenously with ringer lactate solution (400 ml/h) in the PACU. The study outcomes were collected at three assessment periods, 0-0.5 h, 0.5-6 h, 6-24 h, after anesthesia by an independent investigator.
Treatment:
Other: lactated ringers

Trial contacts and locations

1

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Central trial contact

Jiang Liu, B.S

Data sourced from clinicaltrials.gov

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