Hernia. Unilateral inguinal hernia, without obstruction or gangrene
Conditions
Interventions
Intervention 1: Intervention group: Transabdominal laparoscopic preperitoneal surgery method without defect closure. Intervention 2: Control group:Transabdominal laparoscopic preperitoneal surgery met
Sponsors
Rasht University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Unilateral or Bilateral Hernia American Society of Anesthesiologists Risk score (ASA class 1 or 2)
Exclusion criteria
Exclusion criteria: Symptoms of Peritonitis Previous Major Abdominal and Pelvic Surgery Contraindication General Anesthesia or laparoscopy Incarcerated Hernia Strangulated Hernia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Occurrence of complication of Hematoma. Timepoint: 24 hours after the surgery. Method of measurement: Clinical examination.;Occurrence of complication of surgery site infection. Timepoint: One month after surgery. Method of measurement: Clinical examination.;Occurrence of complication of Seroma. Timepoint: One month to 6 months after surgery. Method of measurement: Clinical examination and ultrasound.;Acute postoperative pain. Timepoint: 24 hours after the surgery. Method of measurement: Visual Analogue Scale.;Chronic pain after surgery. Timepoint: 6 months after surgery. Method of measurement: Visual Analogue Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Returning to normal activities. Timepoint: 6 months after surgery. Method of measurement: Patient interview.;Hernia recurrence. Timepoint: 6 months after surgery. Method of measurement: Physical examination. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMoein Moghadam Ahmadi
Rasht University of Medical Sciences
Outcome results
None listed