Clinical trials: Surgical Mesh
Hernia
Peristomal Mesh for Prophylaxis of Parastomal Hernia
The study aims to prove differences or equalities in outcome for patients operated with or without a peristomal mesh in the sublay position when establishing a permanent colostomy.
- Trial name
- NCT00496418
- Testing
- Mesh in permanent colostomy
- Where
- Norway
- Volunteers
- 60 people
- Sponsor
- Oslo University Hospital
Inguinal Hernia, Groin Hernia
A Global Prospective Study on Inguinal Hernia Surgery
The primary aim of the HIPPO study is to identify compliance to audit standards (pre-operative and intraoperative) standards for the repair and management of inguinal hernia.
- Conditions
- Inguinal Hernia, Groin Hernia, Surgery
- Trial name
- HIPPO (NCT05748886)
- Where
- United Kingdom
- Volunteers
- 5,000 people, healthy volunteers welcome
- Sponsor
- University of Birmingham
Hypotension (MeSH: D007022)
Carotid Artery Blood Flow, Blood Pressure, and Cardiac Output During Anesthesia in Children Aged 0-5 Years
Blood pressure is routinely monitored during anesthesia in children, but blood pressure alone may not accurately reflect blood flow to vital organs.
- Trial name
- CARFLOW (NCT07847203)
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Karolinska Institutet
Complete Rectal Prolapse
Laparoscopic Ventral Mesh Rectopexy Versus Delorme's Operation in Management of Complete Rectal Prolapse
A comparative randomized study between laparoscopic ventral mesh Rectopexy and Delorme's procedure in treatment of complete rectal prolapse to ass both efficacy and complications
- Trial name
- NCT02601326
- Testing
- Laparoscopic ventral mesh Rectopexy, Delorme's procedure
- Where
- Egypt
- Volunteers
- 50 people
- Sponsor
- Mansoura University
Pelvic Organ Prolapse Vaginal Surgery, Stress Urinary Incontinence in Women
The AMPER Study: Evaluation of the Efficacy of Human Amniotic Membrane Grafting in Preventing Mesh Exposure in Vaginal Reconstructive Surgery Using Polypropylene Mesh.
This study evaluates the efficacy of adding a human amniotic membrane graft to polypropylene mesh surgery for pelvic prolapse and stress urinary incontinence.
- Trial name
- AMPER (NCT07414849)
- Testing
- Sacrospinous Hysteropexy with Mesh, Retropubic Mid-urethral Sling (Bottom-Up), Transobturator Mid-urethral Sling (Out-In)
- Where
- Argentina
- Volunteers
- 330 people
- Sponsor
- Hospital General de Agudos J. M. Penna
Hysterectomy (MeSH nr: E04.950.300.399)
Transforming Global Surgery Capacity and Capability Through Affordable Virtual Reality
The goal of this randomized controlled trial was to evaluate whether Deliberate Virtual Reality (VR) training can improve surgical skills, knowledge, and confidence in performing postpartum hysterectomy among junior-level Zambian…
- Trial name
- NCT07403526
- Testing
- Deliberate Virtual Reality (VR) Training, Standard Clinical Training
- Where
- Zambia
- Volunteers
- 33 people, healthy volunteers welcome
- Sponsor
- Southern Methodist University
Hernia, Inguinal, Surgical Mesh
Mesh and Mesh Fixation in Laparoscopic Groin Hernia Surgery
The study attempts to quantify the relative risks for recurrence depending on complex combinations of plausible risk factors, in particular mesh, mesh fixation, hernia size and hernia type.
- Conditions
- Hernia, Inguinal, Surgical Mesh, Laparoscopy, Hernia
- Trial name
- NCT03755219
- Testing
- TEP, TAPP
- Volunteers
- 38,450 people
- Sponsor
- Bengt Novik
Liver Cirrhosis
Thoracoscopic Mesh Repair of Diaphragmatic Defects for Hepatic Hydrothorax
The management of refractory hepatic hydrothorax is challenging and usually unsuccessful. The study will discuss the perioperative treatment, effectiveness, and morphology of diaphragmatic defects of hepatic hydrothorax in…
- Trial name
- NCT02508688
- Testing
- thoracoscopic diaphragmatic repair
- Volunteers
- 63 people
- Sponsor
- National Taiwan University Hospital
Complications of Surgical and Medical Care: General Terms
Effective Feedback to Improve Primary Care Prescribing Safety
We hypothesise that feedback and feedback + psychology informed intervention delivered to primary care medical practices will reduce high-risk prescribing to patients compared to a simple educational intervention alone.
- Trial name
- EFIPPS (NCT01602705)
- Testing
- Usual care, Feedback of Performance, Feedback of Performance + Health Psychology Informed Intervention
- Where
- United Kingdom
- Volunteers
- 262 people
- Sponsor
- University of Dundee
Hernia
BP as a Super-light Mesh and as a New Fixation Device for General Surgery -DM108/2008-B
The Buckypaper (BP) is an innovative material that has attracted the attention of many research groups engaged in the study of its possible applications in various technological fields.
- Trial name
- DM108/2008-B (NCT02341222)
- Testing
- BP self-standing felt device, PR Parietene mesh device
- Where
- Italy
- Volunteers
- 30 people
- Sponsor
- University of Roma La Sapienza
Umbilical Hernia
Effect of Reoperation for Recurrence After Open Umbilical Hernia Repair
background Operation for small umbilical hernias is one of the most common surgical procedures, but the best surgical technique, including the choice of suture or mesh remains unknown.
- Trial name
- UMBI-REC (NCT01607801)
- Where
- Denmark
- Volunteers
- 4,847 people
- Sponsor
- Zealand University Hospital
Abdominal Wall Defect, Ventral Hernia
Clinical Study on the Safety of SAFIL® MESH
Observational, Retrospective, Multi-center Clinical Study on the Safety of SAFIL® MESH in Patients Undergoing Reinforcement of Soft Tissues After Abdominal Wall Surgery or Other Fascial Defects
- Conditions
- Abdominal Wall Defect, Ventral Hernia, Abdominal Hernia, Fascial Hernia
- Trial name
- SAFIL_MESH (NCT04947202)
- Testing
- Hernioplasty
- Where
- 2 sites in Spain
- Volunteers
- 152 people
- Sponsor
- Aesculap AG
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
Abdominal Hernia
Light vs Heavy Weighted Mesh Repair in Primary Abdominal Hernia in Terms of Surgical Site Infection
This study compares the incidence of surgical site infections (SSI) in patients undergoing abdominal hernia repair using either light or heavy-weighted polypropylene mesh.
- Trial name
- NCT06644612
- Testing
- Light Weight Mesh, Heavy Weight Mesh
- Where
- Pakistan
- Volunteers
- 106 people
- Sponsor
- Khyber Medical University Peshawar
Hernia, Inguinal, Hernia, Femoral
Chronic Postoperative Pain After the Lichtenstein Groin Hernioplasty
The study attempts to quantify the relative risks for chronic postoperative inguinal pain (CPIP) after Lichtenstein repair of groin hernia, depending on mesh type and fixation suture material.
- Conditions
- Hernia, Inguinal, Hernia, Femoral, Postoperative Pain, Chronic Pain
- Trial name
- NCT04839848
- Testing
- Lichtenstein mesh repair
- Volunteers
- 80,733 people
- Sponsor
- Karolinska Institutet
Spigelian Hernia
Surgical Repair of Spigelian Hernia in a Cohort of Patients
Repair of Spigelian hernias with a tentacle shaped implant and highlighting the results of the procedure
- Trial name
- NCT05379751
- Testing
- Fixation free Spigelian hernia repair with tentacle mesh
- Volunteers
- 54 people
- Sponsor
- University of Cagliari
Urinary Incontinence, Stress
Quality of Life After Tension Free Transvaginal Sling / Tape Operation With a Titanized Surgical Tape (TiLOOP® Tape)
Validation of a new Quality of Life (QoL) questionnaire in a population of patient gaining a TiLOOP® TAPE surgical mesh for stabilization of the urethra.
- Trial name
- NCT01358214
- Testing
- Questionnaire on Quality of Life.
- Where
- Germany
- Volunteers
- 21 people, healthy volunteers welcome
- Sponsor
- pfm medical gmbh
Orbital Fractures, Enophthalmos
Correction of Enophthalmos and Orbital Volume Using Pre-bent Mesh Versus 3d Printed Onlay in Orbital Fracture Cases
this study evaluates the post-surgical correction of enophthalmos and orbital volume using 3D printed only versus pre-bent titanium mesh in blow-out fracture cases
- Conditions
- Orbital Fractures, Enophthalmos, Periorbital Fracture
- Trial name
- NCT04271137
- Testing
- 3D printed PEEK onlay, Pre-bent orbital mesh
- Where
- Egypt
- Volunteers
- 20 people
- Sponsor
- Cairo University
Hernia, Hiatal, Laparoscopic
Laparoscopic Primary Diaphragm Versus Mesh Repair for Hiatus Hernia: a Long-Term Follow-Up
Assessment of the recurrence of hiatal hernia five to ten years after repair using sutures versus sutures reinforced with non-absorbable mesh.
- Conditions
- Hernia, Hiatal, Laparoscopic, Surgery, Recurrence
- Trial name
- PRIME LTFU (NCT05662735)
- Testing
- Mesh repair, Suture repair
- Volunteers
- 60 people
- Sponsor
- Rijnstate Hospital
Spontaneous Pneumothorax, Surgery
Absorbable Mesh Pleurodesis in Thoracoscopic Treatment of Spontaneous Pneumothorax
Primary spontaneous pneumothorax usually occurs in young, lean male without underlying lung disease. In most cases, the cause of pneumothorax is rupture of blebs at the apex of the lung.
- Trial name
- NCT01848860
- Testing
- Thoracoscopic bullectomy and pleural abrasion, Mesh coverage of the staple line
- Where
- Taiwan
- Volunteers
- 204 people
- Sponsor
- National Taiwan University Hospital