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NCT05757986 Clinical Trial

Predictive Model for PONV for Patient Received Gynecological Laparoscopic Surgery

Postoperative Nausea and Vomiting Clinical Trial

Official title:
Dynamic Predictive Model for Postoperative Nausea and Vomiting for Patient Received Gynecological Laparoscopic Surgery

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05757986
Other study ID # 2023YX030
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2022
Est. completion date October 1, 2023

Study information
Verified date June 2023
Source Weifang Medical University
Contact YuXiu Liu, Ph.D
Phone +8618663608162
Email 18663608162@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Recruitment information / eligibility
Status Recruiting
Enrollment 659
Est. completion date October 1, 2023
Est. primary completion date March 1, 2023
Accepts healthy volunteers No
Gender Female
Age group 12 Years and older
Eligibility 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

Related Conditions & MeSH terms

Intervention

Other:
• The presence of nausea and vomiting within 24 hours after surgery
This is a prospective risk prediction model building, thus there is no traditional definition of intervention.

Locations
Country Name City State
China Weifang Medical University Weifang Shangdong

Sponsors (1)
Lead Sponsor Collaborator
Jiang Liu

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary PONV The occurrence and severity of PONV is evaluated by Visual Analogue Scale (VAS). Within 24 hours after surgery
See also
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Completed NCT02449291 - Study of APD421 as PONV Treatment (no Prior Prophylaxis) Phase 3
Recruiting NCT01442012 - Utility of Acupuncture in the Treatment of Postoperative Nausea and Vomiting in Ambulatory Surgery N/A
Completed NCT01478165 - Comparison of TIVA (Total Intravenous Anesthesia) and TIVA Plus Palonosetron in Preventing Postoperative Nausea and Vomiting N/A
Unknown status NCT01268748 - Single Port Versus Four Ports Laparoscopic Cholecystectomy and Early Postoperative Pain N/A
Completed NCT02143531 - Intravenous Haloperidol Versus Ondansetron for Treatment of Established Post-operative Nausea and Vomiting Phase 4
Completed NCT00734929 - Aprepitant With Dexamethasone Versus Ondansetron With Dexamethasone for PONV Prophylaxis in Patients Having Craniotomy Phase 4