Clinical trials: Hernioplasty
Paraesophageal Hernia
Fundoplication in Laparoscopic PEH Repair Based on FLIP
Prospective randomized controlled trial to identify a sub-set of patients that do not benefit from the routine addition, and added morbidity, of a fundoplication during laparoscopic paraesophageal hernia repair.
- Trial name
- PEHFLIP (NCT05807763)
- Testing
- Laparoscopic paraesophageal hernia repair without fundoplication
- Where
- 2 sites in United States
- Volunteers
- 260 people, healthy volunteers welcome
- Sponsor
- The Foundation for Surgical Innovation and Education
Opioid Consumption, Postoperative, ESPB
Evaluation of the Postoperative Efficacy of Bilateral Lumbar Erector Spinae Plane Block (ESPB) in Patients Undergoing Lumbar Disc Herniation Repair Surgery
This prospective observational study aims to evaluate the efficacy of bilateral lumbar erector spinae plane (ESP) block in providing effective postoperative analgesia and its potential impact on early mobilization and length of…
- Conditions
- Opioid Consumption, Postoperative, ESPB, Postoperative Pain, Plane Blocks
- Trial name
- NCT07403734
- Where
- Turkey (Türkiye)
- Volunteers
- 78 people, healthy volunteers welcome
- Sponsor
- Başakşehir Çam & Sakura City Hospital
Ultrasound Guided Rectus Sheath Block, Pain, Postoperative
Comparison Between Ultra Sound Guided Rectus Sheath Block and Field Block for Midline Hernia Repair
Randomized double blinded controlled clinical trial will be done with a total number of 75 patients will be divided into 3 groups.
- Trial name
- NCT03225313
- Testing
- Bupivacaine Hydrochloride 0.5% Injection Solution_#4, Normal Saline Flush, 0.9% Injectable Solution_#5
- Where
- Egypt
- Volunteers
- 75 people, healthy volunteers welcome
- Sponsor
- Theodor Bilharz Research Institute
Ventral Hernia
Risk Factors and Results of Emergency Ventral Hernia Repair
The aim of present study was to evaluate the clinical course after emergency ventral hernia repair in terms of 30-day-readmission, -reoperation and -mortality and to identify risk factors for emergency repair.
- Trial name
- NCT01589276
- Where
- Denmark
- Volunteers
- 10,976 people, healthy volunteers welcome
- Sponsor
- Zealand University Hospital
Hernia, Inguinal
Comparison of Whole Mesh and Split Mesh Use in Laparoscopic Inguinal Hernia Repair
At least 80 patients who will undergo laparoscopic inguinal hernia repair surgery will be randomized into 2 groups. For the patients in the first group, the whole mesh will be laid on the area without being fixed.
- Trial name
- NCT05420376
- Testing
- Split Mesh
- Where
- Turkey (Türkiye)
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- Istanbul Training and Research Hospital
Postoperative Analgesia of Inguinal Hernia Repair in Adults
Subarachnoid Block Versus Ultrasound Guided Transversalis Fascia Plane Block for Postoperative Analgesia of Inguinal Hernia Repair in Adults
The aim of our study is to investigate the effect of the ultrasound guided transversalis fascia plane block on the postoperative opioid consumption as a part of multimodal analgesia in patients undergoing inguinal herniorrhaphy…
- Trial name
- NCT06219837
- Testing
- bupivacaine injection by ultrasound guided transversalis fascia plane block
- Where
- Egypt
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- Cairo University
Incisional Hernia
Risk Factors for Morbidity After Incisional Hernia Repairs
The Danish Ventral Hernia Database (DVHD) registers 37 different perioperative parameters. The aim of present study is to use large-scale data from DVHD to uncover risk factors for readmission, reoperation (any indication), death…
- Trial name
- NCT01430676
- Testing
- differences in surgical techniques
- Where
- Denmark
- Volunteers
- 3,460 people, healthy volunteers welcome
- Sponsor
- Zealand University Hospital
Incisional Ventral Hernia
Cytokine Response to Abdominal Wall Reconstruction
This is a prospective, observational translational study of patients undergoing major abdominal wall reconstruction with primary fascial closure.
- Trial name
- NCT07422584
- Testing
- Not applicable- observational study
- Where
- United States
- Volunteers
- 25 people, healthy volunteers welcome
- Sponsor
- Northwestern University
Inguinal Hernia, Indirect, Children, Only
Inflammatory Stress Response in Pediatric Inguinal Hernia Repair
Today there are various surgical techniques for inguinal hernia. In this study, investigators want to compare the ''PIRS'' operating technique laparoscopy and modified "Marcy" operating technique with open inguinal access.
- Conditions
- Inguinal Hernia, Indirect, Children, Only, Inflammatory Response, Surgery
- Trial name
- NCT03203343
- Testing
- Operation - PIRS, Operation - MARCY
- Where
- Croatia
- Volunteers
- 32 people, healthy volunteers welcome
- Sponsor
- University Hospital of Split
Ventral Incisional Hernia
Open Complex Ventral Incisional Hernia Repair Using Biosynthetic Material for Midline Fascial Closure Reinforcement
Prospective, multicenter, observational study to evaluate performance of GORE® BIO-A® Tissue Reinforcement when used to reinforce midline fascial closure in single-staged open complex ventral incisional hernia repair.
- Trial name
- COBRA (NCT01325792)
- Testing
- GORE® BIO-A® Tissue Reinforcement
- Where
- 9 sites in United States, Netherlands
- Volunteers
- 104 people, healthy volunteers welcome
- Sponsor
- W.L.Gore & Associates
Hernias Inguinal Reducible, Local Anaesthesia
Comparison Between Desarda and Lichtenstein's Technique for Inguinal Hernia Repair Under Local Anaesthesia
Inguinal hernia repair is done by two methods. The conventional method uses a prosthetic mesh for strengthening the defect but has been associated with complications.
- Trial name
- NCT03512366
- Testing
- Desarda's technique, Lichtenstein's technique
- Where
- India
- Volunteers
- 55 people, healthy volunteers welcome
- Sponsor
- All India Institute of Medical Sciences, Bhubaneswar
Groin Hernia
Case Report in Complications After Laparoscopic Transabdominal Preperitoneal Groin Hernia Repair Using LiquiBandFIX8®
This an a case report about management and proving the strenght and resistance of LiquiBandFIX8® using for peritoneal closure in a laparoscopic transabdominal preperitoneal groin hernia repair.
- Trial name
- NCT05952791
- Testing
- Surgery
- Where
- Austria
- Volunteers
- 1 people, healthy volunteers welcome
- Sponsor
- Kepler University Hospital
Ventilation Therapy; Complications
Comparing Different Startegies of Positive Pressure Ventilation in Children
The most basic modes of mechanical ventilation are volume-controlled ventilation (VCV) and pressure-controlled ventilation (PCV).
- Trial name
- NCT06612125
- Testing
- volume controlled ventilation, pressure controlled ventilation, pressure controlled volume grantanteed ventilation
- Where
- Egypt
- Volunteers
- 78 people, healthy volunteers welcome
- Sponsor
- Beni-Suef University
Parastomal Hernia
Outcomes After Parastomal Hernia Repair
The aim of the current study is to evaluate the overall outcomes after parastomal hernia repairs in Denmark from 2007-2017 using data from the Danish Hernia Database and Danish Patients Registry.
- Trial name
- NCT03792243
- Testing
- Complication
- Where
- Denmark
- Volunteers
- 1,062 people, healthy volunteers welcome
- Sponsor
- Zealand University Hospital
Inguinal Hernia
Trial of Laparoscopic Compared to Open Inguinal Hernia Repair in Children Younger Than 3 Years
Laparoscopic techniques have been applied widely to the management of various common pediatric surgical diseases. Current evidence lacks sufficient quality to justify the widespread adoption of the laparoscopic approach to the…
- Trial name
- NCT00716768
- Testing
- Laparoscopic Inguinal Hernia Repair, Open Inguinal Hernia Repair
- Where
- 2 sites in United States
- Volunteers
- 42 people, healthy volunteers welcome
- Sponsor
- Ann & Robert H Lurie Children's Hospital of Chicago
Inguinal Hernia
MR Imaging of the 3D Inguinal Hernia Scaffold ProFlor
Demonstrating through MRI sequuences the regenerative features of the 3D inguinal hernia scaffold ProFlor
- Trial name
- NCT04762264
- Testing
- ProFlor inguinal hernia device
- Where
- Italy
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- University of Cagliari
Choosing Better Drug Option for Sedation in Pediatric Population Intraoperatively
Comparison of Sedative Effect of Dexmedetomidine and Midazolam for TIVA
Comparison of sedative effects of dexmedetomidine and midazolam using ramsay sedation scores intraoperatively in children undergoing inguinal hernia repair.
- Trial name
- NCT05574179
- Testing
- Dexmedetomidine injection, Midazolam
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Sheikh Zayed Medical College
Postoperative Pain, Inguinal Hernia Unilateral
Levobupivacaine and Postoperative Pain Relief
The study analysed direct levobupivacaine instillation in surgical wound and its effectiveness in postoperative pain control. Half participants received 0,5 % levobupivacaine and the other half received 0,9% saline solution
- Trial name
- NCT04869046
- Testing
- Instillation of levobupivacaine in surgical wound
- Where
- 2 sites in Serbia
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Mother and Child Health Institute of Serbia Dr Vukan Cupic
Unilateral Inguinal Hernia With Gangrene and Obstruction
Effectivity of Laparoscopic Inguinal Hernia Repair (TAPP) in Daily Clinical Practice - Early and Long-term Results
The effectiveness of laparoscopic inguinal hernia repair still remains unclear. During a one year period a total of 1208 inguinal hernias in 952 patients were consecutively operated using the laparoscopic technique by a total of…
- Trial name
- NCT02561910
- Testing
- Laparoscopic hernia repair
- Where
- Germany
- Volunteers
- 952 people, healthy volunteers welcome
- Sponsor
- Hernia Center Rottenburg
Hernia, Inguinal
Inversion and Fixation of the Transversalis Fascia in Laparoscopic Inguinal Hernia Repair
According to the EHS classification, at least 80 patients who will undergo TEP repair for the first time with the diagnosis of M2 and M3 direct inguinal hernia will be randomized into 2 groups.
- Trial name
- NCT05420818
- Testing
- Transversalis Fascia Inversion
- Where
- Turkey (Türkiye)
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- Istanbul Training and Research Hospital