ConditionRecurrent Inguinal Hernia
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorThe Second Affiliated Hospital of Kunming Medical University
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
Qualifiers
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
Treatments tested in this trial
- Transabdominal preperitoneal approach
Treatment groups
70 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov