Clinical trials: Mesh
Inguinal Hernia
Can Ideal Mesh Size be Standardized in Open Inguinal Hernia Repair
Two hundred consecutive unilateral inguinal hernia patients will be included in the study. Patients will be recorded by measuring the distance between the pubic tubercle and the deep inguinal ring, the distance between the…
- Trial name
- NCT04280094
- Where
- Turkey (Türkiye)
- Volunteers
- 1 people, healthy volunteers welcome
- Sponsor
- Konya Meram State Hospital
Blow-Out Fractures
Reconstruction of Orbital Floor Blow-out Fractures by Titanium Mesh Versus Autogenous Iliac Graft
Blow-out fractures result from direct blunt impacts to the orbit which causes an immediate rise increase in intra-orbital pressure. Decompression via fracture of the orbital floor then occurs.
- Trial name
- NCT07340879
- Testing
- Titanium mesh, autogenous iliac graft
- Where
- Egypt
- Volunteers
- 80 people
- Sponsor
- Assiut University
Muscle Strength, Postural Balance
The Effects of Whole Body Vibration With Plyometric Training on Physical Performance in Basketball Players
Purpose: The purpose of this study was to determine whether whole body vibration with plyometric training has effect on physical performance parameters and balance also this study searched for if vibration support additional…
- Conditions
- Muscle Strength, Postural Balance, Range of Motion, Articular, Walking Speed, Mesh id D000072797
- Trial name
- WBV (NCT03291483)
- Testing
- whole body vibration, plyometric training
- Where
- Turkey (Türkiye)
- Volunteers
- 24 people, healthy volunteers welcome
- Sponsor
- Hasan Kalyoncu University
Osteoarthritis
A Comparison of Two Surface Materials (Tantalum Versus Titanium Fiber Mesh) of Acetabular Components in Hip Arthroplasty
The purpose of this study is to compare two surface materials (tantalum versus titanium fiber mesh) of acetabular components in hip arthroplasty.
- Trial name
- NCT00116051
- Testing
- Acetabular implant, Monoblock cup
- Where
- Denmark
- Volunteers
- 50 people
- Sponsor
- University of Aarhus
Paraumbilical Hernia
Onlay Mesh Hernioplasty Vs Sublay Mesh Hernioplasty for Paraumbilical Hernia Repair
It is a randomized controlled trial in which we are comparing onlay mesh hernioplasty with sublay mesh hernioplasty for paraumbilical hernia.
- Trial name
- NCT03766061
- Testing
- Onlay mesh Hernioplasty, Sublay Mesh Hernioplasty
- Where
- Pakistan
- Volunteers
- 100 people
- Sponsor
- Services Hospital, Lahore
Inguinal Hernia
Rebound Hernia Repair Device Mesh Trial
This is a post-market study of the Rebound Hernia Repair Device to further establish the safety, efficacy, and utility of the Rebound Hernia Repair Device in a controlled population.
- Trial name
- NCT00968773
- Testing
- Rebound HRD, Standard hernia mesh (VitaMesh)
- Where
- 2 sites in United States
- Volunteers
- 70 people, healthy volunteers welcome
- Sponsor
- Minnesota Medical Development, Inc.
Bone Resorption
Guided Bone Regeneration With Customized Titanium Meshes
The aims of this prospective clinical study are to evaluate: a) the effectiveness of digitally customized titanium meshes in association with autologous bone particles and bovine bone mineral and covered with collagen membranes…
- Trial name
- NCT04480073
- Testing
- Customized CAD-CAM Titanium Mesh (Y-xoss CBR® by Reoss -Filderstadt - Germany) for Guided Bone Regeneration of atrophic alveolar ridges
- Where
- Italy
- Volunteers
- 24 people, healthy volunteers welcome
- Sponsor
- University of Milan
Bone Augmentation, Badly Broken Maxillary Premolars Indicated for Extraction
Comparison of Immediate Implant Placement With Titanium Mesh Versus Collagen Membrane in Type II Socket:
Statement of the problem: Immediate implant placement is faced with several problems. One of the most important issues is dealing with defects in the buccal plate of bone in the esthetic zone.
- Trial name
- NCT06875830
- Testing
- collagen membrane, titanium mesh
- Where
- Egypt
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Misr International University
Ventral Hernia
Sublay Versus Intraperitoneal Onlay Mesh Repair in Large Ventral Hernias
The aims of this study is to compare the efficacy of modified sublay hernioplasty versus intraperitoneal onlay mesh repair for large ventral hernias.
- Trial name
- NCT06643234
- Testing
- Ventral hernia repair
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Ahmed Kahlawy Mahrous Mohamed
Incisional Hernia After Midline Laparotomy
Safety and Efficacy of Prophylactic Re-sorbable Biosynthetic Mesh Following Midline Laparotomy in Clean/Contaminated Field.
The aim of the present study is to analyse the feasibility, safety and IH rate using a prophylactic sublay biosynthetic BIO-A (GORE) mesh in order to prevent incisional hernia following midline laparotomy in clean-contaminated…
- Trial name
- Parthenope (NCT04471311)
- Testing
- Sub-lay mesh supported closure, BIO-A (GORE) mesh
- Where
- Italy
- Volunteers
- 151 people
- Sponsor
- Azienda Sanitaria Locale Napoli 2 Nord
Single Level Stable Thoracolumbar Fracture Type AO A3, Multiple Level Stable Thoracolumbar Fracture Type AO A3
Spine FA3 - a Prospective, International, Multicenter Cohort Study on Treatment of of AO A3 Thoracolumbar Fractures
Thoracolumbar fractures are the most common spinal fractures with an average annual incidence between 18 and 30 per 100'000 inhabitants. The majority of these fractures are AO type A3 ("burst fractures").
- Trial name
- FA3 (NCT01751633)
- Testing
- Surgical, Conservative treatment
- Where
- 8 sites in Brazil, Chile and 4 more
- Volunteers
- 38 people
- Sponsor
- AO Clinical Investigation and Publishing Documentation
Inguinal Hernia
Evaluation of HQ® Matrix Soft Tissue Mesh for the Treatment of Inguinal Hernia
The purpose of the study is to evaluate the safety and effectiveness of HQ® Matrix Soft Tissue Mesh for the Treatment of Inguinal Hernia.
- Trial name
- NCT02487628
- Testing
- HQ® Matrix Soft Tissue Mesh, ULTRAPRO® Partially Absorbable Lightweight Mesh
- Where
- 7 sites in China
- Volunteers
- 144 people
- Sponsor
- Zhejiang Xingyue Biotechnology Co., Ltd.
Chronic Hepatitis C Virus
Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed-Dose Combination ± Ribavirin for the Treatment of HCV (ION-3)
This study is to evaluate the safety, tolerability, and antiviral efficacy of ledipasvir/sofosbuvir (LDV/SOF) fixed-dose combination (FDC) with or without ribavirin (RBV) administered for 8 or 12 weeks in treatment-naive…
- Trial name
- NCT01851330
- Testing
- LDV/SOF, RBV
- Where
- 52 sites in United States
- Volunteers
- 647 people
- Sponsor
- Gilead Sciences
Hernia, Inguinal
Comparative Study on Self-adhesive Mesh for Open Inguinal Hernia Repair
Tension-less mesh repair is the most common procedure for inguinal hernia. Conventional heavy weight polypropylene meshes have been reported to stimulate inflammatory reaction and this is responsible for mesh shrinkage and…
- Trial name
- NCT00960011
- Testing
- PROGRIP, POLYPROPYLENE
- Where
- China
- Volunteers
- 58 people
- Sponsor
- The University of Hong Kong
Herniorrhaphy, Humans
Synthetic Mesh Explant Study
The purpose of this study is to determine whether synthetic hernia mesh materials undergo physical and/or chemical changes while in the body.
- Conditions
- Herniorrhaphy, Humans, Polypropylene, Polytetrafluoroethylene
- Trial name
- NCT01880021
- Where
- United States
- Volunteers
- 111 people
- Sponsor
- Washington University School of Medicine
Hernia, Hiatal
Laparoscopic Repair of Giant Hiatal Hernias With Nitinol-framed Lightweight Polytetrafluoroethylene Mesh
This study is prospective randomized trial enrolling at least 50 participants which compares efficacy and safety of two alternative methods of laparoscopic hiatal repair for giant (i.e.
- Trial name
- GIANT (NCT01780285)
- Testing
- Nitinol-framed lightweight PTFE mesh for hiatal repair, Partially absorbable lightweight mesh for hiatal repair
- Where
- Ukraine
- Volunteers
- 50 people
- Sponsor
- Odessa National Medical University
Abdominal Wall Defect
Study to Evaluate Reduction in Pain After Laparoscopic Hernia Repair With Mesh Soaked in Bupivacaine Solution
Early post-operative pain and discomfort after laparoscopic repair remains a concern for patients requiring hospital stay and parenteral narcotic analgesics .
- Trial name
- HAPPIEST (NCT03035617)
- Testing
- Bupivacaine, Saline
- Where
- Pakistan
- Volunteers
- 100 people
- Sponsor
- Aga Khan University
Concomitant Conditions
Factors Affecting the Improvement of Severity of Concomitant USI After a Novel TVM Surgery for Women With POP
Background/Purpose: A novel transvaginal mesh (TVM) surgery for women with pelvic organ prolapse (POP) had been reported. However, factors affecting the efficacy of this novel TVM surgery are unknown; and the above information…
- Trial name
- NCT03607968
- Testing
- The novel anterior TVM surgeries
- Volunteers
- 134 people
- Sponsor
- National Taiwan University Hospital
Hip Fractures
Geriatric Fracture Centers - Evaluation of a Geriatric Co-management Program
The study will assess patients with at least one major AE related to treatment / hospitalization / immobilization in the Geriatric Fracture Center (GFC) group compared to the usual care group.
- Trial name
- NCT02297581
- Where
- 12 sites in United States, Austria and 4 more
- Volunteers
- 282 people
- Sponsor
- AO Innovation Translation Center
Respiratory Insufficiency
RCT of Mesh Versus Jet Nebulizers on Clinical Outcomes During Mechanical Ventilation in the Intensive Care Unit
Aerosol delivery during mechanical ventilation has long been a long debated topic. As evidence-based knowledge about the delivery of aerosol to the lungs of mechanically ventilated patients increases, one piece of the puzzle has…
- Trial name
- NCT02056119
- Testing
- Vibrating Mesh Nebulizer Arm, Jet Nebulizer Arm
- Where
- United States
- Volunteers
- 120 people
- Sponsor
- Rush University Medical Center