Contribution of PRF in CDH in Children With Prothetic Patch Closure
Condition:   Congenital Diaphragmatic Hernias Intervention:   Biological: Biological functionalization of the prosthetic materials by PRF Sponsor:   University Hospital, Strasbourg, France Not yet recruiting (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - March 4, 2019 Category: Research Source Type: clinical trials

Anterior Component Separation Versus Posterior Component Separation for Repair of Large Ventral Hernias
Condition:   Large Midline Ventral Hernia Interventions:   Procedure: Anterior component separation;   Procedure: Posterior component separation Sponsor:   Zaza Demetrashvili Active, not recruiting (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - January 4, 2019 Category: Research Source Type: clinical trials

Anterior Component Separation Versus Posterior Component Separation for Repair of Large Ventral Hernias
Condition:   Large Midline Ventral Hernia Interventions:   Procedure: Anterior component separation;   Procedure: Posterior component separation Sponsor:   Zaza Demetrashvili Recruiting (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - January 4, 2019 Category: Research Source Type: clinical trials

Anterior Component Separation Versus Posterior Component Separation for Repair of Large Ventral Hernias
Condition:   Large Midline Ventral Hernia Interventions:   Procedure: Anterior component separation;   Procedure: Posterior component separation Sponsor:   Zaza Demetrashvili Active, not recruiting (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - January 4, 2019 Category: Research Source Type: clinical trials

PROphylactic Mesh to Prevent Incisional Hernias at the Former Stoma Site: the PROMISS-trial
Condition:   Incisional Hernia Intervention:   Device: Adhesix® monofilament polypropylene mesh (Bard Davol) Sponsor:   Maastricht University Medical Center Not yet recruiting (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - November 22, 2018 Category: Research Source Type: clinical trials

Preloop trial: study protocol for a randomized controlled trial
DiscussionThis is a pilot trial that will be undertaken to provide some novel evidence on the safety profile and efficiency of both synthetic mesh and biological implants for the prevention of incisional hernias after closure by temporary loop ileostomy. The hypothesis is that synthetic mesh is economical but equally safe and at least as effective as biological implants in hernia prevention and in contaminated surgical sites.Trial RegistrationClinicalTrials.gov,NCT03445936. Registered on 7 February 2018. (Source: Trials)
Source: Trials - November 9, 2018 Category: Research Source Type: clinical trials

Effectiveness of endoscopic totally extraperitoneal (TEP) hernia correction for clinically occult inguinal hernia (EFFECT): study protocol for a randomized controlled trial
The objective of this study is to assess whether watchful waiting is non-inferior to endoscopic totally extraperitoneal (TEP) inguinal repair in patients with a clinically occult inguinal hernia.MethodsThe EFFECT study is a multicenter non-blinded randomized controlled non-inferiority trial. Adult patients with unilateral groin pain and a clinically occult inguinal hernia are eligible to participate in this study. A total of 160 participants will be included and randomized to TEP inguinal hernia repair or a watchful waiting approach. The primary outcome of this study is pain reduction 3  months after treatment, measur...
Source: Trials - June 18, 2018 Category: Research Source Type: clinical trials

Management of Giant Thoracic Disc Hernias by Thoracoscopy: Experience of 52 Cases
Conditions:   Giant Thoracic Herniation;   Myelopathy Intervention:   Procedure: Thoracoscopy Sponsor:   Hopital Foch Completed (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - September 28, 2017 Category: Research Source Type: clinical trials