Clinical trials: Hernia Inguinal
Congenital Hernia
Laparoscopic Recurrent Inguinal Hernia Repair
Laparoscopic management of recurrent inguinal hernia in children has been recently introduced in surgical practice. One of the most important advantages of using the laparoscopic approach in cases with recurrent inguinal hernia…
- Trial name
- NCT04266561
- Testing
- hernia repair
- Where
- Egypt
- Volunteers
- 42 people
- Sponsor
- Al-Azhar University
Postoperative Pain, Inguinal Hernia
No Opioids vs. Minimal Opioids Following Inguinal Hernia Repair
The investigators hypothesize that not prescribing opioids after uncomplicated, outpatient IHR will be non-inferior to prescribing opioids (5 tablets of Oxycodone, 5mg; or surgeon preference for intolerance) with respect to…
- Trial name
- NCT05929937
- Testing
- Opioids, No opioids
- Where
- 8 sites in United States, Canada
- Volunteers
- 904 people
- Sponsor
- Clayton Petro
Inguinal Hernia, Inguinal Hernia Repair
Comparative Study of Inguinodynia After Inguinal Hernia Repair
To evaluate the postoperative pain and the relapse after the repair of the inguinal hernia by Lichtenstein technique with four different mesh types with different types of fixation in patients undergoing major ambulatory surgery.
- Conditions
- Inguinal Hernia, Inguinal Hernia Repair, Open Inguinal Hernia
- Trial name
- NCT03678272
- Testing
- HERNIOPLASTY WITH PANAVALE MESH, HERNIOPLASTY WITH PARIETEX PROGRIP MESH, HERNIOPLASTY WITH ADHESIX MESH
- Volunteers
- 270 people
- Sponsor
- Hospital General Universitario Elche
Inguinal Hernias
Ilioinguinal Nerve Block With Local Anesthetic vs. Placebo in Inguinal Hernia Repair Under Spinal Anesthesia
Postoperative pain management remains a critical area of concern in surgical practices, especially in procedures involving the lower abdomen and pelvis.
- Trial name
- NCT07049835
- Testing
- Ilioinguinal/iliohypogastric Nerve Block
- Where
- Lebanon
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Makassed General Hospital
Analgesia
Comparing the Efficacy of Ultrasound Guided Erector Spinae Plane Block, Ultrasound Guided Caudal Block, and Local Infiltration for Postoperative Pain Control in Pediatric Patients Undergoing Unilateral Inguinal Hernia Repair as a Day-Case Surgeries: A Randomized Controlled Trial
The aim of this study is to evaluate the efficacy of ultrasound guided Erector block versus caudal block versus local wound infiltration perioperatively according to: Primary outcome: to assess and compare the postoperative…
- Trial name
- ECLU (NCT06849804)
- Testing
- Erector Spinae (ESP) Block with Bupivacaine (Marcaine®), Caudal Block Anesthesia, Local infiltration in the wound
- Where
- Egypt
- Volunteers
- 75 people, healthy volunteers welcome
- Sponsor
- Tanta University
Indirect Inguinal Hernia, Pediatric
Comparative Study of Needlescopic Inguinal Hernia Repair Versus Open Herniotomy
This study aims to compare between two techniques to treat hernia in children which are Needlescopic inguinal hernia repair and Open classic surgery as regard operative time, cosmetic appearance, recurrence and other complications
- Trial name
- Needlescopic (NCT06936423)
- Testing
- Open herniotomy, Needlescopic percutaneous Internal ring suturing
- Where
- Egypt
- Volunteers
- 43 people
- Sponsor
- Ain Shams University
Sedation During Spinal Anesthesia
Sedation During Spinal Anesthesia
Patients during spinal anesthesia should be sedated.
- Trial name
- NCT03133780
- Testing
- Ketamine, Midazolam
- Where
- Egypt
- Volunteers
- 80 people
- Sponsor
- Assiut University
Hernia, Inguinal
Use of Pre-peritoneal Drainage in rTAPP - a Comparative Study
The safety and efficacy of pre-peritoneal drain after TEP has been validated in our previous studies - which can effectively reduce seroma formation post-operatively and safe in clinical use.
- Trial name
- DrainrTAPP (NCT04960267)
- Testing
- Use of pre-peritoneal drainage after rTAPP
- Where
- China
- Volunteers
- 50 people
- Sponsor
- The University of Hong Kong
Pain, Beta-endorphin
Double-blind, Randomized Controlled Study to Assess the Analgesic Effect of 2 g of Magnesium Dipyrone (Metamizol) and Changes in Plasma Beta-endorphin Immunoreactivity Values in Patients Undergoing Elective Inguinal Herniorrhaphy Under Epidural Anesthesia.
A double-blind, randomized controlled study is designed to assess the analgesic effect of a single intravenous dose of 2 g of magnesium dipyrone (metamizol) and whether the administration of the active drug will be associated…
- Conditions
- Pain, Beta-endorphin, Dipyrone, Hernia Surgery
- Trial name
- NCT04595877
- Testing
- Dipyrone administration, Pain assessment, beta-endorphin immunoreactivity
- Where
- Spain
- Volunteers
- 60 people
- Sponsor
- Antonio Martín Duce
Inguinal Hernia
Paravertebral Blocks: Pilot Study to Compare Nerve Stimulation vs. Anatomic Landmarks in Inguinal Hernia Repair
Primary aim: 1. To compare the nerve stimulation vs. anatomic techniques of paravertebral block of T11-L1 in providing surgical anesthesia for patients undergoing inguinal hernia repair. Secondary aims: 1.
- Trial name
- PVB (NCT00587704)
- Testing
- PVB using nerve stimulation, PVB using anatomic landmarks
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- Mayo Clinic
Hernia, Inguinal
Parietex Progrip Study
The objective of the study is to evaluate pain and disabling complications inducing social consequences in primary inguinal hernia ProGrip mesh repair compared to Lichtenstein repair with lightweight polypropylene mesh.
- Trial name
- NCT00827944
- Testing
- Parietex Progrip, Low weight polypropylene mesh
- Where
- 9 sites in Belgium, Germany and 3 more
- Volunteers
- 603 people
- Sponsor
- Medtronic - MITG
Inguinal Hernia
Effect of Ultra-Sound Guided Pre-emptive Nerve Block on Post-operative Pain Following Open Inguinal Hernia Repair.
A hernia occurs when an organ 'like intestines' or fatty tissue protrude through a weak point in muscle or connective tissue and one of the most common types of hernia is inguinal.
- Trial name
- NCT04792164
- Testing
- Ultra sound guided nerve block, Usual infiltration
- Volunteers
- 136 people
- Sponsor
- Imam Abdulrahman Bin Faisal University
Inguinal Hernia
Multicentric Evaluation of UPP, UHS and Ultra Pro Comfort Plug for Inguinal Hernia Surgery Including Quality of Life Evaluation
Outpatient services in Germany are less controlled by external quality assurance programs. Comprehensive outcome data for benchmarking or health-care decision-making are missing e.g. for day case surgery.
- Trial name
- NCT02315209
- Testing
- UHS, UPP, Comfort Plug
- Volunteers
- 4,000 people
- Sponsor
- University of Magdeburg
Emergency Inguinal Hernia Repair, Emergency Ventral Hernia Repair
Emergency Hernia Repair
Emergency hernia repairs are associated with significantly higher morbidity and mortality compared with elective hernia surgery.
- Trial name
- NCT07314398
- Testing
- Emergency hernia repair
- Volunteers
- 600 people
- Sponsor
- Oulu University Hospital
Inguinal Hernia
Day Case Inguinal Hernia Repair in Children. Is Laparoscopic Approach Justified?
We compare laparoscopic and classic open operation for inguinal hernia in children. Attention is focused on the recovery, surgical result and the duration of the operation and hospital stay.
- Trial name
- NCT00597194
- Testing
- Hernia repair
- Where
- Finland
- Volunteers
- 89 people
- Sponsor
- Hospital for Children and Adolescents, Finland
Inguinal Hernia Repair, Umbilical Hernia Repair
Robotic Single Port Combined Umbilical and Inguinal Hernia Repair
Evaluation of the perioperative and patient reported outcomes of a new surgical technique: robotic inguinal hernia repair using the Da Vinci SP system.
- Trial name
- CAPPUCCINOH (NCT07755696)
- Testing
- da Vinci Single Port Surgical System, Robotic Single-Port Inguinal and Concomitant Umbilical Hernia Repair
- Where
- Belgium
- Volunteers
- 30 people
- Sponsor
- Algemeen Ziekenhuis Maria Middelares
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
Inguinal Hernia
Phase I/II Dose-escalation Study to Evaluate Safety, PK and Efficacy of TLC590 for Postsurgical Pain Management
Phase I/II, randomized, double-blind, comparator-controlled, dose-escalation study to assess the safety, PK, and efficacy of single postsurgical application of TLC590 compared with Naropin®
- Trial name
- NCT03591146
- Testing
- TLC590, Naropin
- Where
- United States
- Volunteers
- 65 people
- Sponsor
- Taiwan Liposome Company
Inguinal Hernia
Antibiotic Prophylaxis in Mesh Repair of Inguinal Hernias
Inguinal hernia repairs is clean surgical procedures. However infection may be a concern when prosthetic materials are used. This prospective randomized study has been set to observe if antibiotic prohylaxis is of benefit in mesh…
- Trial name
- NCT01264003
- Testing
- sefazolin
- Volunteers
- 200 people
- Sponsor
- Diskapi Teaching and Research Hospital
Inguinal Hernia, Ventral Hernia
Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fixation Device With Deep Purchase Tacks
A post-market clinical follow-up study for ReliaTack™ articulating reloadable fixation device with deep purchase tacks
- Trial name
- RAFDT (NCT03526341)
- Testing
- ReliaTack™ Articulating Reloadable Fixation Device
- Where
- United States
- Volunteers
- 116 people
- Sponsor
- Medtronic - MITG