Umbilical Hernia

3

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

Condition / disease
Location
Status: Recruiting

Ultrasound-Guided Transversus Abdominis Plane Block Versus Epidural Block for Umbilical Hernia Analgesia

This observational study aims to compare the postoperative analgesic effectiveness of ultrasound-guided transversus abdominis plane (TAP) block and single-dose epidural anesthesia in patients undergoing umbilical hernia surgery. Pain intensity will be assessed using the Visual Analog Scale (VAS) at predefined postoperative time points. The study seeks to determine which analgesic approach provides superior pain control and patient satisfaction in the postoperative period.

Participants needed: 30
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Sakarya UniversityUpdated: Jun 24, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Patients aged 18 to 65 years [+5]

ASA physical status III or higher [+9]

Status: Recruiting

Ultrasound Guided External Oblique and Rectus Abdominis Plane Block (EXORA) on Neuroendocrine Stress Response in Adults Undergoing Umbilical Hernia Surgery

This study aims to evaluate the efficacy of ultrasound-guided external oblique and rectus abdominis plane block on the neuroendocrine stress response and postoperative analgesia in adults undergoing umbilical hernia repair.

Participants needed: 100
Trial details
Age: 21-65Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jan 8, 2026Locations: 1
Eligibility criteria

Aged from 21 to 65 years. [+3]

ASA Ⅲ or Ⅳ. [+8]

Status: Recruiting

Factors Influencing the Results of Treatment in Patients With Hernias of Various Localizations

The study attempts to quantify the relative risks for acute postoperative pain, complications rate, chronic postoperative pain (CPIP) and recurrence rate after different methods of repair of groin, umbilical and incisional hernia depending on surgical technique, mesh type and fixation suture material. For this purpose the investigators will analyze data from the Kalinigrad Hernia Registry (KHR).

Participants needed: 4,000
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: Immanuel Kant Baltic Federal UniversityUpdated: Jul 23, 2024Locations: 1
Eligibility criteria

All mesh and non-mesh repairs that have been registered in the KHR from January...

Patients not having a 11-digit state-assigned Personal insurance policy number. [+2]