317 studies found for:    "abdominal wall defect" OR "Hernia, Abdominal"
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Rank Status Study
21 Active, not recruiting "BP as a New Device for Surgery and Solid Cancer and Hematopoietic System Tumors Treatment. Effects of BP Implantation"
Conditions: Hernia of Abdominal Wall;   Incisional Hernia
Interventions: Procedure: BP selfstanding felt;   Procedure: PP mesh;   Procedure: BP intraperitoneal mesh;   Procedure: control group
22 Unknown  Case-control Study of Mesh-infection After a Size Tailored Hernia Repair With C-Qur V-Patch
Conditions: Ventral Hernia;   Umbilical Hernia;   Epigastric Hernia;   Trocar-site Hernia
Intervention: Procedure: primary ventral hernia repair with mesh
23 Terminated Prospective Study Of A Size Tailored Approach To Repair Umbilical And Epigastric Primary Ventral Hernias
Conditions: Ventral Hernia;   Umbilical Hernia;   Epigastric Hernia
Intervention:
24 Recruiting Multi-Center Study To Examine The Use Of Flex HD® And Strattice In The Repair Of Large Abdominal Wall Hernias
Condition: Hernia of Abdominal Wall
Interventions: Device: FLEX-HD;   Device: Strattice
25 Recruiting Prospective Trial Comparing the Performance Profiles of Two Non-Cross-Linked Porcine Dermal Matrices in Abdominal Wall Reconstruction
Conditions: Hernia, Ventral;   Intestinal Fistula;   Fibromatosis, Abdominal
Interventions: Procedure: Abdominal wall reconstruction with Strattice;   Other: Assess pain intensity at last office visit preoperatively;   Other: Assess pain interference at last office visit preoperatively;   Other: Assess physical functioning at last office visit preoperatively;   Other: Assess patient quality of life at last office visit preoperatively;   Other: Assess patient pain intensity postoperatively;   Other: Assess pain interference postoperatively;   Other: Assess physical functioning postoperatively;   Other: Assess quality of life postoperatively;   Other: Assess hernia recurrence at 30 days postoperatively;   Other: Assess bulge at 30 days postoperatively;   Other: Assess Surgical Site Occurrences at 30 days postoperatively;   Other: Assess hernia recurrence at 1 year postoperatively;   Other: Assess bulge at 1 year postoperatively;   Other: Assess Surgical Site Occurrences at 1 year postoperatively;   Other: Assess overall complications at 30 days postoperatively;   Other: Assess overall complications at 1 year postoperatively;   Procedure: Abdominal wall reconstruction with XenMatrix;   Device: Strattice;   Device: XenMatrix
26 Recruiting Safety of Mesh Used Repairs in Emergency Abdominal Wall Hernias. Prospective Randomized Multicenter Trial
Condition: Hernia
Intervention: Procedure: inguinal hernia repair
27 Completed Laparoscopic Intraperitoneal Mesh Repair of Ventral Hernia: Comparison to Conventional Mesh Repair
Condition: Hernia, Ventral
Intervention: Other: laparoscopic
28 Enrolling by invitation Abdominal Wall Repair With Strattice in Germany: a Cohort Study
Conditions: Hernia of Abdominal Wall;   Biologic Mesh;   Strattice
Intervention: Procedure: Complex abdominal wall repair Strattice
29 Completed The Permacol Dutch Cohort Study
Conditions: Hernia of Abdominal Wall;   Biologic Implant;   Infected Hernioplasty Mesh
Intervention: Procedure: Permacol mesh placement
30 Completed Safety Study of MotifMESH (cPTFE) in Abdominal Surgery
Condition: Hernia
Intervention: Device: MotifMESH
31 Not yet recruiting Mesh Fixation With a Synthetic Glue in Primary Inguinal Hernia Repair
Condition: Inguinal Hernia
Intervention:
32 Not yet recruiting PVB With vs. Without Clonidine for Ventral Hernia Repair
Condition: Ventral Hernia Repair
Interventions: Other: Clonidine;   Other: Placebo
33 Recruiting A Pilot Study to Investigate the Safety, Efficacy, Pharmacokinetics and Bioavailability of HTX-011 Administered Via Injection or Topical Application Following Unilateral Open Inguinal Herniorrhaphy
Condition: Analgesia in Patients With Inguinal Herniorrhaphy
Interventions: Drug: HTX-011-19;   Drug: Placebo
34 Completed Single-centre Single-blinded Randomised Study Evaluating the Impact of Mesh Pore Size on Chronic Pain After Lichtenstein Hernioplasty
Condition: Inguinal Hernia Repair
Interventions: Device: Optilene LP mesh;   Device: Ultrapro mesh
35 Recruiting Evaluation of HQ® Matrix Soft Tissue Mesh for the Treatment of Inguinal Hernia
Condition: Inguinal Hernia
Interventions: Device: HQ® Matrix Soft Tissue Mesh;   Device: ULTRAPRO® Partially Absorbable Lightweight Mesh
36 Recruiting Effects of Preoperative Relaxation and Intensified Surgery Education in Patients Undergoing Herniotomy
Conditions: Hernia, Inguinal;   Anxiety;   Postoperative Pain
Interventions: Behavioral: relaxation program;   Behavioral: surgery education
37 Active, not recruiting Use of Acellular Dermal in the Incarcerated Inguinal Hernia Tension-free Reconstructions
Condition: Incarcerated Inguinal Hernia
Intervention: Procedure: ADM tension-free hernia reparation
38 Recruiting Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Mesh Fixation
Conditions: Inguinal Hernia;   Pain
Interventions: Device: Parietex ProGrib self-fixating mesh;   Device: Tack fixation
39 Recruiting Mesh Fixation and Closure of Peritoneum Following Laparoscopic Hernia Repair Using N-butyl Cyanoacrylate
Condition: Hernia, Inguinal
Intervention: Device: LiquiBandFix8
40 Recruiting Non-Op Management of Ventral Hernia Patients
Condition: Hernia, Ventral
Intervention:

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Indicates status has not been verified in more than two years