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Predictive Model for PONV for Patient Received Gynecological Laparoscopic Surgery

J

Jiang Liu

Status

Enrolling

Conditions

Postoperative Nausea and Vomiting

Treatments

Other: The presence of nausea and vomiting within 24 hours after surgery

Study type

Observational

Funder types

Other

Identifiers

NCT05757986
2023YX030

Details and patient eligibility

About

This is a prospective study to dynamically predict the risk of PONV in patients undergoing gynecologic laparoscopic surgery.

Enrollment

659 estimated patients

Sex

Female

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

-All female patients receiving gynecological laparoscopic surgery.

Exclusion criteria

-Patients requiring intraoperative open-surgery, requiring other procedures in addition to gynecological laparoscopy, with severe organ dysfunction, unstable postoperative vital signs or requiring transfer to ICU.

Trial design

659 participants in 2 patient groups

Experimental group
Treatment:
Other: The presence of nausea and vomiting within 24 hours after surgery
Control group
Treatment:
Other: The presence of nausea and vomiting within 24 hours after surgery

Trial contacts and locations

1

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Central trial contact

YuXiu Liu, Ph.D

Data sourced from clinicaltrials.gov

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