Comparing ligament preservation and removal in hernia surgery for women

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

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 it's running

• Nanchong Central Hospital
  Nanchong, Sichuan, China Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.