Comparing ligament preservation and removal in hernia surgery for women
Comparative Study on the Effect of Uterine Round Ligament Preservation Vs Resection in Laparoscopic Inguinal Hernia Repair in Women： a Multicenter,Stratified Randomized Controlled Trial
This study is trying to see if keeping or removing a specific ligament during hernia surgery helps women recover faster and have fewer problems afterward.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 466 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Nanchong Central Hospital Government |
| Locations | 1 site (Nanchong, Sichuan) |
| Trial ID | NCT06885788 on ClinicalTrials.gov |
What this trial studies
This study compares the clinical effects of preserving versus resecting the uterine round ligament during laparoscopic inguinal hernia repair in women. It aims to evaluate the time required for surgery as the primary outcome, while secondary outcomes include hernia recurrence rates, quality of life assessments, and indicators of postoperative recovery. The study involves female patients diagnosed with unilateral inguinal hernia and will be conducted at Nanchong Central Hospital.
Who should consider this trial
Good fit: Ideal candidates are female patients over 18 years old diagnosed with unilateral inguinal hernia who do not have childbearing requirements.
Not a fit: Patients with severe comorbidities or those who are pregnant or lactating may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical outcomes and recovery for women undergoing inguinal hernia repair.
How similar studies have performed: There is limited information on similar studies, making this approach relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ►Age : Female patients over 18 years of age without a childbearing requirement * Diagnosis and basis : Female patients diagnosed with Unilateral inguinal hernia. * agreed to participate in this study and signed the informed consent form. Exclusion Criteria: * ►Combined with severe heart, liver, kidney and other diseases. * pregnant or lactating women. * those with surgical contraindications.
Where this trial is running
Nanchong, Sichuan
- Nanchong Central Hospital — Nanchong, Sichuan, China (Recruiting)
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.