Laparoscopic Inguinal Hernia Repair

2

Review clinical trials related to Laparoscopic Inguinal Hernia Repair. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Individualized vs Standard PEEP and Oxygen Reserve Index in Laparoscopic Hernia Surgery

During laparoscopic surgery under general anesthesia, lung function can be affected by increased abdominal pressure and patient positioning. Positive end-expiratory pressure (PEEP) is a ventilator setting that helps keep the lungs open during surgery. In standard practice, a fixed PEEP level is applied to all patients. An individualized PEEP approach tailors this setting to each patient based on lung recruitment maneuvers. This study investigates whether individualized PEEP improves oxygenation compared to standard PEEP in patients undergoing laparoscopic inguinal hernia surgery. Oxygenation will be continuously monitored using the Oxygen Reserve Index (ORI), a non-invasive sensor. Lung aeration will also be assessed before and after surgery using bedside lung ultrasound.

Participants needed: 60
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Fatih Sultan Mehmet Training and Research HospitalUpdated: Aug 20, 2026Locations: 1
Eligibility criteria

Aged 18-75 years [+4]

Age below 18 or above 75 years [+13]

Status: Not yet recruiting

Transversalis Fascia Plane Block Versus M-TAPA Block After Laparoscopic Inguinal Hernia Repair

This randomized clinical trial aims to evaluate and compare the analgesic efficacy of the Transversalis Fascia Plane Block (TFPB) and the Modified Thoracoabdominal Nerve Block through Perichondrial Approach (M-TAPA) in patients undergoing laparoscopic inguinal hernia repair. The primary outcome is the Visual Analog Scale (VAS) score within the first 24 hours after surgery. Secondary outcomes include total opioid consumption, requirement for rescue analgesia, block-related complications and adverse effects (hematoma, local anesthetic systemic complications, vascular puncture, and infection), patient satisfaction assessed using a Likert scale, quality of recovery assessed using the QoR-15 questionnaire, and incidence of postoperative nausea and vomiting.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Antalya City HospitalUpdated: Jun 1, 2026
Eligibility criteria

Patients aged 18-65 years [+5]

Refusal to participate [+8]