Predictive Model for PONV for Patient Received Gynecological Laparoscopic Surgery

Recruiting

• Conditions: Postoperative Nausea and Vomiting
• Interventions: Other: The presence of nausea and vomiting within 24 hours after surgery

• Registration Number: NCT05757986
• Lead Sponsor: Jiang Liu

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2022-09-01
• Study First Submitted: 2023-02-22
• Primary Completion: 2023-03-01
• Study First Submitted QC: 2023-03-03
• Study First Posted: 2023-03-07
• Status Verified: 2023-06
• Last Update Submitted: 2023-06-13
• Last Update Posted: 2023-06-15
• Study Completion: 2023-10-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: Female
• Target Recruitment: 659

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.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Experimental group	The presence of nausea and vomiting within 24 hours after surgery	-
Control group	The presence of nausea and vomiting within 24 hours after surgery	-

Primary Outcome Measures

Name	Time	Method
PONV	Within 24 hours after surgery	The occurrence and severity of PONV is evaluated by Visual Analogue Scale (VAS).

Trial Locations

Locations (1)

Weifang Medical University; 🇨🇳 Weifang, Shangdong, China