Clinical trials: Mesh
Horizontal Alveolar Bone Loss
Horizontal Ridge Augmentation Using Polyvinylidene Fluoride Versus Titanium Mesh Membranes
This study aims to evaluate the effectiveness of a new PVDF non-resorbable membrane versus Titanium Mesh in the treatment of horizontal ridge defects prepared for implant placement
- Trial name
- PVDF + HRA (NCT07095530)
- Testing
- titanium membrane
- Where
- Egypt
- Volunteers
- 42 people, healthy volunteers welcome
- Sponsor
- Minia University
Incisional Hernia/Prevention and Control
Prometheus: Prophylactic Mesh After OLtx for Hernia Reduction Study.
A multicenter prospective, consecutive case series study, on the use of a bio-absorbable mesh for prevention of incisional hernia, in high risk patients, after orthotopic liver transplantation.
- Trial name
- PROMETHEUS (NCT07744230)
- Testing
- mesh
- Where
- Italy
- Volunteers
- 100 people
- Sponsor
- University of Rome Tor Vergata
Breast Cancer
Brass Mesh Bolus in Rotational Post-Mastectomy Radiation Therapy
The hypothesis is that the daily use of brass mesh bolus achieves a comparable dose to every-other-day use of Superflab bolus (current standard of care) in chest wall post-mastectomy patients treated with rotational 6 MV photon…
- Trial name
- NCT05483712
- Testing
- Brass Mesh Bolus
- Where
- Canada
- Volunteers
- 20 people
- Sponsor
- Nova Scotia Cancer Centre
Incisional Hernia Occurence
Primary Mesh Closure of Abdominal Midline Wounds
Incisional hernia is the most frequently seen long term complication in surgery causing much morbidity and even mortality in patients.
- Trial name
- PRIMA (NCT00761475)
- Testing
- mesh supported closure, primary closure
- Where
- 12 sites in Austria, Germany and 1 more
- Volunteers
- 480 people
- Sponsor
- Erasmus Medical Center
MeSH
Comparison of the Effectiveness of Sambiloto Herbs (Andrographis Paniculata) and Brisk Walking Exercise on Blood Glucose of Obese Patients
Problem Formulation 1. Does herbal medicine sambiloto affect the blood glucose levels of obese sufferers? 2. Does brisk walking affect blood glucose levels in obese sufferers? 3.
- Trial name
- NCT06520501
- Testing
- Herbal Medicine Sambiloto, Brisk Walking, Brisk Walking and Herbal Medicine Sambiloto
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Universitas Palangka Raya
COPD
Aerogen Nebuliser Versus Standard Nebulised Therapy in Acute Chronic Obstructive Pulmonary Disease
The investigators are looking at whether a new type of nebuliser (a machine used to deliver drugs to the airways) is better at delivering drugs to the lungs of people with Chronic Obstructive Pulmonary Disease (COPD), compared…
- Trial name
- NCT02379065
- Testing
- The Aerogen Aeroneb Solo©, Phillips Respironic© mask
- Where
- United Kingdom
- Volunteers
- 22 people
- Sponsor
- Chelsea and Westminster NHS Foundation Trust
Stress Urinary Incontinence
Autologous Versus Synthetic Versus Biological Sling for Trans-obturator Correction of Urinary Stress Incontinence
The treatment of urinary stress incontinence with trans-obturator approach, know as transobturatory tape (TOT), is a largely used sling-adopting procedures.
- Trial name
- NCT00744198
- Testing
- Autologous transobturator tape procedure, Synthetic transobturator tape procedure, Biological transobturator tape procedure
- Where
- Italy
- Volunteers
- 8 people
- Sponsor
- University Magna Graecia
Cystocele
UGYTEX® Mesh Versus Subvesical Plication in the Surgical Treatment of Bladder Prolapse
The main purpose of this study is to evaluate the long-term (5-8 years) functional prolapse recurrence rate of the 147 patients enrolled, randomized and analyzed in the study PRO-CURE I.
- Trial name
- PRO-CURE II (NCT02255994)
- Testing
- UGYTEX, No mesh.
- Where
- 12 sites in France
- Volunteers
- 75 people
- Sponsor
- Centre Hospitalier Universitaire de Nīmes
Incisional Hernia, Large Incisional Hernia
Retrospective Analysis on Large Incisional Hernia in High Risk Patients
Large incisional hernia (LIH) is a challenging condition where the abdominal wall is hopelessly compromised. Nowadays the best treatment option in this particularly frail subset of patients is a major issue.
- Trial name
- NCT04801394
- Testing
- hernioplastic and insertion of FLaPp® composite mesh
- Volunteers
- 43 people
- Sponsor
- University of Campania Luigi Vanvitelli
Abdominal Wall Defect, Abdominal Wall Infection
The Use of Synthetic Mesh in Contaminated and Infected Abdominal Wall Repairs. A Long-term Prospective Clinical Trial
Background: Abdominal wall reconstruction in patients presenting with enteric fistulas and mesh infection is challenging. There is a consensus that synthetic mesh must be avoided in infected operations.
- Conditions
- Abdominal Wall Defect, Abdominal Wall Infection, Abdominal Wall Fistula, Infection
- Trial name
- NCT03702153
- Testing
- Abdominal wall reconstruction
- Where
- Brazil
- Volunteers
- 80 people
- Sponsor
- University of Sao Paulo General Hospital
Normal Subjects
Radioaerossol Pulmonary Deposition Using Mesh in Normal Subjects
In vivo deposition studies of aerosol administration during noninvasive ventilation are scarce in the current literature. We assessed 10 normal subjects in a crossover study evaluated by pulmonary scintigraphy aiming to compare…
- Trial name
- NCT01889524
- Testing
- Mesh nebulizer, Jet nebulizer, Noninvasive ventilation-NIV
- Where
- Brazil
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- Universidade Federal de Pernambuco
Inguinal Hernia
MESH MIGRATION IN TOTAL EXTRAPERITONEAL INGUINAL HERNI REPAIR
Inguinal henri repair is among the most common operations performed by general surgery. The use of laparoscopy in inguinal hernia repair is becoming more common day by day.
- Trial name
- NCT05655988
- Testing
- inguinal ultrasonography
- Where
- Turkey (Türkiye)
- Volunteers
- 72 people
- Sponsor
- Fatih Sultan Mehmet Training and Research Hospital
Orbital Deformity
Titanium Mesh Coated With Natural Hydroxyapatite Nanocrystals in Orbital Reconstruction
Reconstruction of maxillofacial continuity defects has always been a challenging task for scientists and surgeons over the years.
- Trial name
- NCT05437731
- Testing
- Coated titanium mesh, Uncoated titanium mesh
- Where
- Egypt
- Volunteers
- 12 people
- Sponsor
- Hams Hamed Abdelrahman
Segmental Long Bone Defects
Comparative Efficacy of the Masquelet Versus Titanium Mesh Cage Techniques for the Treatment of Large Long Bone Defects
The United States Department of Defense (DoD) is funding exciting new research at the University of Texas Medical Branch (UTMB) Department of Orthopaedic Surgery and Rehabilitation that can be a major improvement in the treatment…
- Trial name
- NCT02015390
- Testing
- Autogenous RIA bone grafting, Allogeneic bone grafting
- Where
- United States
- Volunteers
- 16 people
- Sponsor
- The University of Texas Medical Branch, Galveston
Pelvic Organ Prolapse
Comparisons of Clinical Outcomes Between Novel Tailored Transvaginal Mesh Surgery and Vaginal Native Tissue Repair Surgery for Pelvic Organ Prolapse
The issue of whether utilizing the mesh in the surgical treatment of pelvic organ prolapse remained undetermined.Thus, the aim of this study is to analyze clinical outcome of women who underwent pelvic organ prolapse surgeries…
- Trial name
- NCT02465710
- Testing
- Pelvic organ prolapse surgery without mesh, Pelvic organ prolapse surgery with mesh
- Where
- Taiwan
- Volunteers
- 350 people
- Sponsor
- National Taiwan University Hospital
Proctitis, Proctosigmoiditis
The Safety and Tolerability of Budesonide Foam in Participants With Active Ulcerative Proctitis or Proctosigmoiditis
The purpose of this study is to evaluate safety and tolerability of cyclically-dosed rectal budesonide foam in participants with active ulcerative proctitis (UP) or ulcerative proctosigmoiditis (UPS).
- Trial name
- NCT01349673
- Testing
- Budesonide Foam
- Where
- United States
- Volunteers
- 114 people
- Sponsor
- Bausch Health Americas, Inc.
Pelvic Organ Prolapse
Vaginal Uphold Hysteropexy and Laparoscopic Sacral Hysteropexy for the Treatment of Uterovaginal Pelvic Organ Prolapse
The purpose of this study is to evaluate surgical success or failure one year after surgery for pelvic organ prolapse.
- Trial name
- VAULT (NCT01377142)
- Testing
- Laparoscopic sacral hysteropexy, Vaginal mesh hysteropexy
- Where
- 8 sites in United States, Canada
- Volunteers
- 148 people
- Sponsor
- The Cleveland Clinic
Post-operative Neurosurgery
Scintigraphic Comparison of Lung Deposition With Two Nebulizers During Invasive Mechanical Ventilation
Many devices are available for nebulising drug solution during invasive mechanical ventilation. Vibrating-mesh nebulizers ensure the highest lung deposition output.
- Trial name
- NCT02450279
- Testing
- technetium-99m - Diethylenetriaminepentaacetic acid, Vibrating-mesh nebulizer, Jet Nebulizer
- Where
- Belgium
- Volunteers
- 20 people
- Sponsor
- Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Incisional Hernia, Pelvic Cancer
Trial of Collagen Mesh for Prevention of Ventral Hernia After Surgery for Advanced Pelvic Cancer
The aim of the present project is to investigate whether use of biological mesh at the donor site of the rotation flap in closure of the abdominal wall reduce the frequency of incisional hernia formation compared to the usual…
- Trial name
- VRAM (NCT00647569)
- Testing
- Mesh repair, Conventional facial closure
- Where
- Denmark
- Volunteers
- 59 people
- Sponsor
- University of Aarhus
Postoperative Pain, Recurrence
Desarda Repair Compared to Lichtenstein Repair for the Treatment of Inguinal Hernias
The Lichtenstein technique for hernia repair is safe and simple, but the underlying mesh prosthesis has its setbacks, as it acts as a mechanical barrier5.
- Conditions
- Postoperative Pain, Recurrence, Wound Complication
- Trial name
- NCT04850131
- Testing
- Desarda repair
- Where
- Pakistan
- Volunteers
- 82 people, healthy volunteers welcome
- Sponsor
- Benazir Bhutto Hospital, Rawalpindi