Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorNanchong Central Hospital
About this trial
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.
Eligibility criteria
Qualifiers
►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.
Disqualifiers
►Combined with severe heart, liver, kidney and other diseases.
pregnant or lactating women.
those with surgical contraindications.
Trial design
Treatments tested in this trial
- To remove the uterine uterine ligament
Treatment groups
466 Participants
are divided into 8 treatment groups8
Treatment groupsSee each treatment group below.
Sponsors and collaborators
Source ClinicalTrials.gov