Using snap-needle therapy and ginger paste to improve recovery after gynecologic surgery
Effect of Using Snap-Needle Therapy in Combination With Ginger Paste During Anesthesia Recovery on the Recovery of Gastrointestinal Function After Gynecologic Laparoscopy
NA · Weifang Medical University · NCT06320613
This study is testing if using snap-needle therapy along with ginger paste can help women recover better from gynecologic surgery by reducing nausea and improving digestion.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 150 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | Female |
| Sponsor | Weifang Medical University (other) |
| Locations | 1 site (Weifang, Shandong) |
| Trial ID | NCT06320613 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of combining snap-needle therapy with ginger paste during the recovery phase from anesthesia in patients undergoing gynecologic laparoscopy. The approach aims to enhance gastrointestinal function and reduce postoperative nausea and vomiting (PONV). Patients will receive acupuncture therapy and a ginger acupuncture point patch as part of their recovery process. The study focuses on patients classified as ASA I or II who are undergoing general anesthesia for gynecologic procedures.
Who should consider this trial
Good fit: Ideal candidates are patients aged between 18 and 65 undergoing gynecologic laparoscopic procedures under general anesthesia.
Not a fit: Patients with a history of postoperative nausea and vomiting, digestive disorders, or allergies to ginger may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve gastrointestinal recovery and reduce nausea for patients after gynecologic surgery.
How similar studies have performed: While similar approaches have been explored, this specific combination of therapies is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. ASA I or II; 2. Performing gynecologic laparoscopic procedures under general anesthesia; Exclusion Criteria: 1. Age ≤ 18 or ≥65; 2. The patient has a previous history of PONV, digestive disorders, etc; 3. Ulcers, infections, and skin tears at acupressure and acupuncture (snap-needle) treatment sites; 4. Patients allergic to ginger； 5. Inability to follow protocol or refusal to participant
Where this trial is running
Weifang, Shandong
- Lin Cheng — Weifang, Shandong, China (RECRUITING)
Study contacts
- Principal investigator: Lin Cheng, B.S — Weifang People's Hospital
- Study coordinator: Lin Cheng, B.S
- Email: 1318216353@qq.com
- Phone: 17667404256
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.
Conditions: Gastrointestinal Motility, Postoperative Nausea and Vomiting, Recovery of Function, PONV