308 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 Terminated Prospective Study Of A Size Tailored Approach To Repair Umbilical And Epigastric Primary Ventral Hernias
Conditions: Ventral Hernia;   Umbilical Hernia;   Epigastric Hernia
Intervention:
23 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
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 Completed The Permacol Dutch Cohort Study
Conditions: Hernia of Abdominal Wall;   Biologic Implant;   Infected Hernioplasty Mesh
Intervention: Procedure: Permacol mesh placement
29 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
30 Completed Safety Study of MotifMESH (cPTFE) in Abdominal Surgery
Condition: Hernia
Intervention: Device: MotifMESH
31 Recruiting Progrip Ventral Study for Sublay Repair
Condition: Primary Ventral and Incisional Hernia Repair.
Intervention: Device: Parietex ProGrip™
32 Completed LACH-Trial: LAparoscopic Correction of Hernia
Conditions: Incisional Hernia;   Ventral Hernia
Intervention: Procedure: laparoscopic correction of hernia with mesh
33 Completed Hernia Repair Four Arm Comparative Study
Condition: Inguinal Hernia
Interventions: Procedure: open properitoneal hernia repair;   Procedure: Lechtestien hernia repair;   Procedure: Laparoscopic transperitoneal approach;   Procedure: Laparoscopic totally extraperitoneal approach
34 Completed
Has Results
Dose-ranging Study for Postoperative Analgesia in Subjects Undergoing Primary Unilateral Inguinal Hernia Repair
Condition: Postoperative Pain
Interventions: Drug: Bupivacaine HCl;   Drug: SKY0402
35 Recruiting The Flemish Umbilical Nitinol Mesh Trial, a Multicenter Trial
Condition: Umbilical Hernia
Interventions: Procedure: Intraperitoneal mesh placement;   Procedure: Preperitoneal mesh placement
36 Enrolling by invitation Caudal Versus Rectus Sheath Study
Condition: Umbilical Hernia
Intervention: Drug: Bupivacaine
37 Recruiting Transversus Abdominis Plane Block and Inguinal Hernia Repair
Conditions: Inguinal Hernia;   Abdominal Wall Muscles;   Regional Anesthesia;   Postoperative Pain
Intervention: Procedure: Transversus abdominis plane block
38 Completed Strattice in Repair of Inguinal Hernias
Condition: Hernia, Inguinal
Interventions: Device: Inguinal hernia repair with Ultrapro;   Device: Inguinal hernia repair with Strattice
39 Completed The Addition of Clonidine to 0.2% Ropivacaine for Wound Instillation After Minor Lower Abdominal Surgery in Children
Conditions: Hernia, Inguinal;   Hydrocele
Intervention: Drug: clonidine
40 Suspended Local Anaesthetic Following Hernia Repair
Condition: Inguinal Hernias
Intervention: Drug: Ropivicaine

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Indicates status has not been verified in more than two years