Combining acupuncture with regional anesthesia for pain relief after hysterectomy
Benefit of Acupuncture Combined to Regional Analgesia for Post Operative Pain Relief After Hysterectomy
This study is testing if adding acupuncture to a common pain relief method can help women feel less pain and recover better after having a hysterectomy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 72 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | Female |
| Sponsor | Vinmec Healthcare System Academic / other |
| Locations | 1 site (Hanoi) |
| Trial ID | NCT06002464 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the effectiveness of combining acupuncture with bilateral continuous erector spinae plane block (ESPB) for postoperative pain relief in women undergoing elective hysterectomy. Patients will be randomly assigned to receive either the ESPB alone or the ESPB combined with acupuncture. The study aims to evaluate the benefits of this combined approach in reducing pain and improving recovery outcomes. The trial will be conducted at VinMec International Hospital in Hanoi.
Who should consider this trial
Good fit: Ideal candidates for this study are women scheduled for elective hysterectomy who are willing to participate and provide informed consent.
Not a fit: Patients who may not benefit include those with allergies to local anesthetics, mental deficits, or substance abuse issues.
Why it matters
Potential benefit: If successful, this approach could significantly enhance postoperative pain management and improve recovery experiences for patients.
How similar studies have performed: While the combination of acupuncture and regional anesthesia is a novel approach, similar studies have shown promising results in pain management.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * female * elective hysterectomy * accept ton participate * signed consent Exclusion Criteria: * patient refusal * allergy to local anesthetics * complex congenital malformation * mental deficit * substance abuse(alcohol, drugs, opioids) * renal insufficiency
Where this trial is running
Hanoi
- Vinmec international hospital — Hanoi, Vietnam (Recruiting)
Study contacts
- Principal investigator: Philippe Macaire, MD — Vinmec Healthcare System
- Study coordinator: Huyen Vu
- Email: v.huyenvx@vinmec.com
- Phone: (024)39750028
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.