N/A N=299 Lichtenstein Patch or Prolene Hernia System (PHS) for Inguinal Hernia Repair
Chronic Pain
Primary: Long-term Sequelae — 10; 13 percentage of participants
Clinical Trial Search
Completed trials with posted results — search by concept, filter by the parameters that matter at the bedside.
N/A N=100 Inguinal Hernia Study Using Biodesign IHM
Inguinal Hernia
Primary: Number of Patients With Inguinal Hernia Recurrence — 3; 0 participants — p=0.11
Phase 4 N=172 Strattice in Repair of Inguinal Hernias
Hernia, Inguinal
Primary: Change From Baseline in Activities Assessment Scale at 3 Months — -7.49; -6.12 units on a scale
N/A N=124 Modified "Open Intraperitoneal Mesh" Technique of Incisional Ventral Hernia Repair
Incisional Ventral Hernia · Recurrent Ventral Hernia
Primary: Number of Early Postoperative Complications (Wound Infections, Seroma, Hematoma) — 9; 21; 2; 92 participants
N/A N=15 Neo-nervegenesis in Inguinal Hernia Implant ProFlor
Inguinal Hernia
Primary: Ingrowth of Newly Formed Nervous Elements Within Hernia Implant ProFlor — 999.75; 1044; 2094 μm^2 — p=0.028
N/A N=58 Comparative Study on Self-adhesive Mesh for Open Inguinal Hernia Repair
Hernia, Inguinal
Primary: Operating Time From Skin Incision to Wound Closure — 39.2; 47.7 minutes
N/A N=34 Mesh Fixation and Closure of Peritoneum Following Laparoscopic Hernia Repair Using N-butyl Cyanoacrylate
Hernia, Inguinal
Primary: Number of Participants With Safe Fixation of Mesh and Closure of Peritoneum by Clinical Investigation During Hospital Stay and Telephone Interview at Six Weeks…
N/A N=75 Laparoscopic vs. Robotic Ventral Hernia Repair With IPOM
Ventral Hernia
Primary: Postoperative Pain Scores — 5; 5; 4; 3 score on a scale
N/A N=126 A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using Parietex™ Composite Ventral Patch
Hernia
Primary: Primary Hernia Recurrence Rate at 24 Month Follow-up. — 3 Participants
N/A N=119 Study Of Hernia Repair Utilizing The Bard Ventrio Hernia Patch
Ventral Hernia
Primary: The Primary Endpoint is the Rate of Hernia Recurrence in Study Patients. — 0 participants
N/A N=92 Ventral Hernia Study Using OviTex Reinforced Bioscaffold
Hernia, Ventral
Primary: Surgical Site Occurrences or Wound-related Events — 0; 10; 3; 4 Participants
N/A N=101 Open Versus Robotic Retromuscular Ventral Hernia Repair
Ventral Hernia
Primary: Composite Outcome of Diagnosis of Surgical Site Occurrence or Infection, Hospital Readmission, or Hernia Recurrence — 9; 9 Participants
N/A N=41 Miromatrix Biological Mesh for Hiatal Hernia Repair
Hiatal Hernia
Primary: Number of Subjects With a Hernia Recurrence Requiring Reoperation — 0 Participants
Phase 4 N=120 Parastomal Reinforcement With Strattice
Parastomal Hernia
Primary: Occurrence of Parastomal Hernia in Subjects Undergoing Permanent Abdominal Wall Ostomy Creation With and Without Strattice Fascial Inlay. — 6; 7 participants
N/A N=9 SurgiMend Mesh at the Hiatus
Hiatal Hernia
Primary: Recurrence Rate — 6; 3 Participants
N/A N=75 Prospective Trial Comparing Two Different Polypropylene Meshes for Inguinal Hernias
Hernia, Inguinal
Primary: Inguinal Hernia Mesh Insertion Times — 9.76; 8.70 Minutes — p=0.523
N/A N=30 Prospective Clinical Evaluation of High-Purity Type I Collagen in Select High-Risk Hernia Repair Scenarios
Hernia · Ventral Hernia · Incisional Hernia
Primary: Number of Participants With Early Postoperative Safety Events (Surgical Site Infection, Mesh-Related Adverse Events, or Reoperation) — 4; 0; 0; 0 Participants
N/A N=253 Biologic Mesh Versus Synthetic Mesh in Repair of Ventral Hernias
Ventral Hernia
Primary: Number of Participants With Absence of Surgical Site Occurrence Requiring Procedural Intervention — 124; 126; 2; 1 Participants
Phase 2 N=63 Phase 2 Herniorrhaphy Study for Opioid Elimination
Postoperative Pain
Primary: Percentage of Subjects Receiving no Opioid Rescue — 30; 27 Participants
N/A N=104 Open Complex Ventral Incisional Hernia Repair Using Biosynthetic Material for Midline Fascial Closure Reinforcement
Ventral Incisional Hernia
Primary: Hernia Recurrence Rate — 17.3 % of subjects with recurrent hernia
N/A N=334 Effect of Suture for Mesh Fixation in Lichtenstein Hernia Repair
Inguinal Hernia
Primary: Pain, Numbness and Discomfort in the Groin — 28; 34 participants
N/A N=38 Tacking Mesh Versus Self-fixating Mesh for Inguinal Hernia Repair
Hernia, Inguinal
Primary: Mean Operative Time — 69; 84; 40; 66 minutes — p=0.17
N/A N=112 Stoma Closure and Reinforcement Trial
Colon Cancer · Rectal Cancer · Ileostomy - Stoma
Primary: Number of Participants With Wound Occurrences — 0 Participants
Phase 4 N=603 Parietex Progrip Study
Hernia, Inguinal
Primary: Pain Assessment During the First Three Months and at One Year After Surgery Using a Visual Analogue Scale (VAS) — 7.48; 6.76; 4.62; 5.27 units on a scale
N/A N=145 Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair
Ventral Hernia
Primary: Number of Participants With Hernia Recurrence Within 12 Months Following Parietene™ DS Composite Mesh Use in Ventral Hernia Repair — 4; 116 Participants
N/A N=120 A Prospective Trial of a Bio-absorbable Mesh in Challenging Laparoscopic Ventral or Incisional Hernia Repair
Hernia, Ventral · Incisional Hernia
Primary: Surgical Site Occurrence Rate — 1 subjects
N/A N=143 Study Evaluating the Impact of Mesh Pore Size on Chronic Pain After Lichtenstein Hernioplasty
Inguinal Hernia
Primary: Chronic Pain — 34.3; 46.3 percentage of patients with pain
N/A N=200 TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh
Postoperative Complications
Primary: Proportion of Subjects Who Experience Hernia Recurrence (Defect Treated Initially With Parietex™ ProGrip™) Within 12 Months Post-surgery. — 3 participants
N/A N=83 Repair of Infected or Contaminated Hernias
Hernia
Primary: Incidence of Wound Events — 53 participants
Phase 4 N=216 AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repair
Hernia, Inguinal · Hernia, Ventral
Primary: Postoperative Pain — .8; 2.0; 2.2; 3.3 units on a scale