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
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 466
- Locations
- 1
- Primary Endpoint
- Time required for patient surgery
Study Overview
Brief Summary
This study aims to compare the clinical effects of uterine round ligament preservation versus resection in laparoscopic inguinal hernia repair in women.The primary outcomes included Time required for patient surgery.The secondary outcomes included Inguinal hernia recurrence,quality of life assessment,Indicators of postoperative recovery,, et al.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- Double (Participant, Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
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.
Arms & Interventions
Patients with unilateral hernia who did not give birth,the uterine round ligament resection group
Both groups underwent laparoscopic inguinal hernia repair,the resection group removed the uterine round ligament.(Patients with unilateral hernia who did not give birth)
Intervention: To remove the uterine uterine ligament (Procedure)
Patients with unilateral hernia who did not give birth,the uterine round ligament preservation group
Both groups underwent laparoscopic inguinal hernia repair,the preservation group retained the uterine round ligament.(Patients with unilateral hernia who did not give birth)
Patients with unilateral hernia who have given birth,the uterine round ligament resection group
Both groups underwent laparoscopic inguinal hernia repair,the resection group removed the uterine round ligament.(Patients with unilateral hernia who have given birth)
Intervention: To remove the uterine uterine ligament (Procedure)
Patients with unilateral hernia who have given birth,the uterine round ligament preservation group
Both groups underwent laparoscopic inguinal hernia repair,the preservation group retained the uterine round ligament.(Patients with unilateral hernia who have given birth)
Patients with bilateral hernias who have given birth,the uterine round ligament resection group
Both groups underwent laparoscopic inguinal hernia repair,the resection group removed the uterine round ligament.(Patients with bilateral hernias who have given birth)
Intervention: To remove the uterine uterine ligament (Procedure)
Patients with bilateral hernias who have given birth,the uterine round ligament preservation group
Both groups underwent laparoscopic inguinal hernia repair,the preservation group retained the uterine round ligament.(Patients with bilateral hernias who have given birth)
Patients with bilateral hernia who did not give birth,the uterine round ligament resection group
Both groups underwent laparoscopic inguinal hernia repair,the resection group removed the uterine round ligament.(Patients with bilateral hernia who did not give birth)
Intervention: To remove the uterine uterine ligament (Procedure)
Patients with bilateral hernia who did not give birth,the uterine round ligament preservation group
Both groups underwent laparoscopic inguinal hernia repair,the preservation group retained the uterine round ligament.(Patients with bilateral hernia who did not give birth)
Outcomes
Primary Outcomes
Time required for patient surgery
Time Frame: 20-120minutes
Time required for patient surgery
Secondary Outcomes
- Inguinal hernia recurrence(1 month, 3 months, 6 months,1year,2years,3years,6years)
- Quality of life assessment(3 months,6months,1year,2years,3years,6years)