Clinical trials: Hernia Repair
Darn Vs. Lichtenstein Hernia Outcomes, Outcomes of Darn and Lichtenstein Hernia Repairs
Comparing Darn and Lichtenstein Repair for Bilateral Inguinal Hernias in Adult Males in a Low-Resource Setting
This retrospective study evaluates the efficacy of Darn versus Lichtenstein repair methods in treating bilateral inguinal hernias in adult males within a low-resource setting in Sudan.
- Conditions
- Darn Vs. Lichtenstein Hernia Outcomes, Outcomes of Darn and Lichtenstein Hernia Repairs, Bilateral Inguinal Hernia: Darn Vs. Lichtenstein
- Trial name
- NCT06681454
- Where
- Sudan
- Volunteers
- 75 people
- Sponsor
- Sudan Medical Specialization Board
Inguinal Hernia
Modified Guarnieri-Desarda Technique Versus Lichtenstein Technique in Inguinal Hernia Repair
The aim of this study is to compare the surgical outcome of both Lichnichtien tension free mesh hernioplasty of inguinal hernia and the combined modified Guarnieri Desarda technique in terms of postoperative pain, post operative…
- Trial name
- NCT06595628
- Testing
- Lichtenstein Mesh-Based Hernioplasty, Combined Modified Guarnieri-Desarda Tissue-Based Hernioplasty
- Where
- Egypt
- Volunteers
- 40 people
- Sponsor
- Cairo University
Acute Pain
Evaluation of the Analgesic Efficacy of Multimodal Pain Control Regimens That Aim to Limit the Use of Narcotics in Cholecystectomy and Hernia Repairs
Subjects were patients of the five surgeons with Surgical Associates of Mansfield (SAM) who underwent an elective or urgent laparoscopic cholecystectomy; or elective or urgent laparoscopic or open hernia repair (inguinal…
- Trial name
- NCT06095453
- Testing
- Pain control regimens
- Where
- United States
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Methodist Health System
Ventral Hernia, Umbilical Hernia
Preperitoneal Umbilical Mesh Area
The aim of this study is to measure the mesh shrinkage and the visualization of the mesh with MRI scan at 1 month and 13 months after robot assisted preperitoneal hernia repair using the visible CICAT mesh (Dynamesh®).
- Conditions
- Ventral Hernia, Umbilical Hernia, Ventral Incisional Hernia
- Trial name
- PUMA (NCT05576753)
- Testing
- Hernia repair
- Where
- Belgium
- Volunteers
- 20 people
- Sponsor
- Algemeen Ziekenhuis Maria Middelares
Pain, Postoperative, Inguinal Hernia Unilateral
Intrathecal Morphine and Transversalis Fascia Plane Block for Analgesia After Open Inguinal Hernia Repair
Inguinal hernia is a common surgical condition, and open inguinal hernia repair may be associated with significant postoperative pain.
- Conditions
- Pain, Postoperative, Inguinal Hernia Unilateral, Intrathecal Morphine, Transversalis Fascia Plane Block
- Trial name
- NCT07826741
- Testing
- Intrathecal Morphine Group, Transversalis Fascia Plane Block Group, Control Group
- Where
- Turkey (Türkiye)
- Volunteers
- 90 people
- Sponsor
- Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
Incisional Hernia
The Effect of Postoperative Abdominal Binder to Improve Outcomes After Incisional Hernia Repair
Postoperative seroma formation is one of the most common complications after ventral hernia repair with mesh. Although some seromas may not have clinical impact postoperative seroma formation often causes pain and discomfort and…
- Trial name
- INSAB (NCT01776775)
- Testing
- Abdominal binder
- Where
- Denmark
- Sponsor
- Hvidovre University Hospital
Laparoscopic Inguinal Hernia Repair
Laparoscopic Inguinal Hernia Repair TEP vs TAPP
This study is dedicated to compare between 2 different techniques is the management of inguinal hernia repair using laparoscopic intervention and how it may affect the patients life style covering both benefits and possible…
- Trial name
- NCT07108972
- Testing
- Transabdominal pre-peritoneal laparoscopic inguinal hernia repair, Totally extraperitoneal laparoscopic inguinal hernia repair
- Where
- Egypt
- Volunteers
- 60 people
- Sponsor
- Sohag University
Recovery of Postoperative
The Effect of Erector Spina Plan Block Application Time on Postoperative Anxiety
we aimed to compare the effect of preoperative awake or post-induction erector spina plane block on patient anxiety and recovery quality in patients who will undergo elective lumbar disc hernioplasty.
- Trial name
- NCT05406128
- Testing
- preoperative erector spina plane block, intraoperative erector spina plane block
- Where
- Turkey (Türkiye)
- Volunteers
- 108 people, healthy volunteers welcome
- Sponsor
- Ankara City Hospital Bilkent
Hernia, Inguinal, Inguinal Hernia, Direct
Study of Laparoscopic Inguinal Hernia Repair
Although mesh fixation has been associated to an increased incidence of nerve injury and involves increased operative costs, many surgeons feel that fixation is necessary to reduce the risk of hernia recurrence.
- Conditions
- Hernia, Inguinal, Inguinal Hernia, Direct, Inguinal Hernia, Indirect, Hernia, Femoral
- Trial name
- NCT02920307
- Testing
- TEP without fixation, TEP with fixation, TAPP without fixation
- Where
- Turkey (Türkiye)
- Volunteers
- 400 people
- Sponsor
- Medical Park Gaziantep Hospital
Acute Pain
The Effect of Lidocaine Patch for Postoperative Pain
The lidocaine patch is currently only permitted for post herpetic neuralgia but the investigators want to study its effectiveness in post operative pain after inguinal herniorrhaphy
- Trial name
- NCT04754451
- Testing
- Group L
- Where
- South Korea
- Volunteers
- 32 people
- Sponsor
- BON WOOK KOO
Hernia, Inguinal, Postoperative Pain
Comparison of Hernia Sac Ligation Versus Invagination
Management of indirect hernial sac in inguinal hernia repairs has long been a subject of debate among general surgeons. Although hernial sac high ligation (HL) is a time-honored concept in groin hernia surgery…
- Conditions
- Hernia, Inguinal, Postoperative Pain, Recurrence
- Trial name
- NCT05308251
- Testing
- Lichtenstein Mesh Hernioplasty
- Where
- Turkey (Türkiye)
- Volunteers
- 108 people
- Sponsor
- Samsun Education and Research Hospital
Inguinal Hernia, Circumcision
Analgesia in Children Using Caudal Epidural Ropivacaine
Caudal epidural analgesia (caudal block)is used in standard pediatric anesthesia practice. It has been shown to be effective in managing postoperative pain in children undergoing abdominal and infraumbilical surgery (Tobias et al…
- Trial name
- NCT01494272
- Where
- 2 sites in United States
- Volunteers
- 90 people, healthy volunteers welcome
- Sponsor
- Loma Linda University
Surgical Site Infections
Continuous v Bolus Infusion of Cefazolin During Ventral Hernia Repair
Patients undergoing an elective ventral hernia repair will be randomly assigned to receive either bolus infusion or continuous infusion of the cefazolin as the prophylactic antibiotic.
- Trial name
- NCT02666365
- Testing
- Bolus infusion of Cefazolin, Continuous infusion of Cefazolin
- Sponsor
- Milton S. Hershey Medical Center
Inguinal Hernias
Polypropylene Meshes in Hernia Repair
The aim of this study was to analyze the shrinkage of two different screens in the repair of inguinal hernias in men . 32 patients with unilateral inguinal hernia were assigned randomly.
- Trial name
- NCT01090219
- Testing
- two different meshes in the repair of inguinal hernias
- Where
- 2 sites in Brazil
- Volunteers
- 32 people
- Sponsor
- Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude
Ventral Hernia, Ventral Incisional Hernia
Open Preperitoneal Mesh Versus Retromuscular Mesh Versus Suture Repair for Abdominal Wall Hernias
Randomized clinical trial comparing open preperitoneal mesh, retromuscular mesh and suture repair for ventral hernias less than 3 cm diameter
- Conditions
- Ventral Hernia, Ventral Incisional Hernia, Umbilical Hernia
- Trial name
- NCT03255239
- Testing
- Ventral hernia repair
- Where
- Tunisia
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Hôpital Universitaire Taher Sfar
Hernia of Abdominal Wall, Biologic Implant
The Permacol Dutch Cohort Study
Incisional hernia is the most frequently seen long term complication in surgery causing much morbidity and even mortality in patients.
- Conditions
- Hernia of Abdominal Wall, Biologic Implant, Infected Hernioplasty Mesh
- Trial name
- NCT02166112
- Testing
- Permacol mesh placement
- Where
- 24 sites in Netherlands
- Volunteers
- 77 people
- Sponsor
- Erasmus Medical Center
Inguinal Hernia
Neo-nervegenesis in Inguinal Hernia Implant ProFlor
The investigation is aimed at specifically demonstrating the ingrowth of newly formed nervous elements within a 3D dynamic responsive implant for inguinal hernia repair.
- Trial name
- NCT04171102
- Testing
- ProFlor Hernia implant
- Volunteers
- 15 people, healthy volunteers welcome
- Sponsor
- University of Cagliari
Inguinal Hernia
Mesh Fixation inTEP Inguinal Hernia Repair
Mesh fixation is used to prevent recurrence in TEP to the potential cost of pain. The aim was to evaluate the impact of permanent fixation (PF) versus non-permanent fixation (N-PF) of mesh in TEP repair for a primary inguinal…
- Trial name
- register (NCT02419950)
- Testing
- Fixation of mesh in TEP
- Where
- Sweden
- Volunteers
- 1,110 people
- Sponsor
- Skane University Hospital
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
Inguinal Hernia Unilateral, Erector Spinae Plane Block
Effect of Preoperative Erector Spinae Plane Block on Recovery Quality, Time to Return to Daily Activities, and Postoperative Pain Scores in Inguinal Hernia Surgery
This study aims to evaluate the effect of the erector spinae plane block (ESPB), performed after surgery, on quality of recovery, postoperative pain, and time to return to daily activities in patients undergoing open inguinal…
- Conditions
- Inguinal Hernia Unilateral, Erector Spinae Plane Block, Quality of Recovery (QoR-15), Numeric Rating Scale
- Trial name
- ESPB for IHR (NCT07509957)
- Testing
- Erector Spinae Plane Block (ESPB) group
- Where
- 2 sites in Turkey (Türkiye)
- Volunteers
- 60 people
- Sponsor
- Sanliurfa Education and Research Hospital