Predicting nausea and vomiting after gynecological laparoscopic surgery
Dynamic Predictive Model for Postoperative Nausea and Vomiting for Patient Received Gynecological Laparoscopic Surgery
This study is trying to find out which women are more likely to experience nausea and vomiting after having laparoscopic surgery for gynecological issues, so doctors can better manage these symptoms.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 659 (estimated) |
| Ages | 12 Years and up |
| Sex | Female |
| Sponsor | Weifang Medical University Academic / other |
| Locations | 1 site (Weifang, Shangdong) |
| Trial ID | NCT05757986 on ClinicalTrials.gov |
What this trial studies
This observational study aims to develop a predictive model for postoperative nausea and vomiting (PONV) in female patients undergoing gynecological laparoscopic surgery. By monitoring patients for the presence of nausea and vomiting within 24 hours post-surgery, the study seeks to identify risk factors that contribute to PONV. The approach involves collecting data from a prospective cohort to enhance understanding and prediction of PONV occurrences. This could lead to improved management strategies for affected patients.
Who should consider this trial
Good fit: Ideal candidates for this study are female patients scheduled for gynecological laparoscopic surgery.
Not a fit: Patients requiring open surgery or those with severe organ dysfunction or unstable vital signs may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could help reduce the incidence of postoperative nausea and vomiting, leading to better recovery experiences for patients.
How similar studies have performed: Other studies have shown success in predicting PONV using various models, indicating that this approach has potential for effectiveness.
Eligibility criteria
Show full inclusion / exclusion criteria
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.
Where this trial is running
Weifang, Shangdong
- Weifang Medical University — Weifang, Shangdong, China (Recruiting)
Study contacts
- Study coordinator: YuXiu Liu, Ph.D
- Email: 18663608162@163.com
- Phone: +8618663608162
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.