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Uterine Round Ligament Preservation Vs Resection in Laparoscopic Inguinal Hernia Repair in Women:A Multicenter,Stratified Randomized Controlled Trial

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06885788
Enrollment
466
Registered
2025-03-20
Start date
2024-09-20
Completion date
2027-03-01
Last updated
2025-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inguinal Hernia, Laparoscopic Surgery, Randomized Controlled Trial

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.

Interventions

PROCEDURETo remove the uterine uterine ligament

Both groups underwent laparoscopic inguinal hernia repair. The preservation group retained the uterine round ligament, while the resection group had it removed.

Sponsors

Nanchong Central Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
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.

Design outcomes

Primary

MeasureTime frameDescription
Time required for patient surgery20-120minutesTime required for patient surgery

Secondary

MeasureTime frameDescription
Inguinal hernia recurrence1 month, 3 months, 6 months,1year,2years,3years,6yearsthe recurrence of inguinal hernia
Quality of life assessment3 months,6months,1year,2years,3years,6yearsQuality of life assessment:The international general quality of life scale (such as SF - 36, etc.) is used to evaluate the quality of life of patients at 3 months , 6months,1year,2years,3years and 6years after surgery.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026