About this trial
The objective of this study was to explore the clinical efficacy of transabdominal preperitoneal approach (TAPP) and open tension-free hernia repair in the treatment of recurrent inguinal hernia. This study aims to provide a basis for selecting the optimal treatment methods for recurrent hernias.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
age ≥ 18 years
the diagnosis of recurrent inguinal hernia made by ultrasound or computed tomography (CT) during the present visit
ability to tolerate general anesthesia and local anesthesia surgery
all patients and their families agreed to participate in this study and sign relevant informed consent.
Disqualifiers
patch infection during the first surgery
multiple (≥ 2) relapses
inability to cooperate to complete follow-up after surgery
Trial design
Parallel
Treatments tested in this trial
Transabdominal preperitoneal approach
Procedure/SurgeryThe enrolled patients underwent either open tension-free hernia repair or Transabdominal preperitoneal approach
Treatment groups
Trial outcomes
Primary outcomes
Postoperation pain
Postoperative pain was monitored using the VAS pain scoring system (0-10 points) and recorded at 24 and 48 h. Patients with groin pain for more than 3 months were recorded during follow-up.
Secondary outcomes
Numbness and foreign body sensation
The occurrence of groin numbness and foreign body sensation after operation was recorded
Operating time
Record the patient\'s operating time
Hemorrhage
The amount of surgical bleeding was recorded
Urinary retention
Urinary retention was observed and recorded after operation
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