N/A N=402 Evaluation of Surgisis Gold Graft for Incision Reinforcement After Open Bariatric Surgery
Hernia · Obesity
Primary: Incisional Hernia — 32; 38 participants — p=0.60
Clinical Trial Search
Completed trials with posted results — search by concept, filter by the parameters that matter at the bedside.
Phase 4 N=40 Comparison of Excision Versus Punch Incision in the Treatment of Epidermal Cysts
Epidermal Cyst
Primary: Number of Participants With Cyst Recurrence — 3; 2 participants
N/A N=4 Efficacy Study to Evaluate Laparoscopic Fascial Closure Device
Hernia, Abdominal
Primary: Count of Participants With Successful Port Site Closure Using Port Close Device — 3 Participants
N/A N=56 Orthopaedic Surgical Wound Closure Comparison Study
Incision, Surgical
Primary: Stony Brook Scar Evaluation Scale — 2.8; 4.09; 3.45 score on a scale
N/A N=20 PEAK PlasmaBlade™ vs. Traditional Electrosurgery in Abdominoplasty
Elastosis
Primary: Acute Thermal Injury Depth — 195; 763 micrometers — p=<0.001
N/A N=12 Clinical Evaluation of the GLYDe Dressing for Post-surgical Incision Care
Post Surgical Incisions From Abdominoplasty Procedures
Primary: Scar Evaluation at End of Treatment Period Comparing Treated to Standard of Care (Control) — 18.64; 50.52 score on a scale
N/A N=96 Scalpel vs Diathermy in Repeat Cesarean Delivery
Complications; Cesarean Section
Primary: Incision Time . — 271.5; 188.17 Seconds — p=<0.001
N/A N=702 Prospective, Randomized, Parallel-arm Clinical Trial of CleanCision or Alexis O in Elective Colorectal Surgery
Colorectal Surgery
Primary: Surgical Site Infection (SSI) Rate — 16; 14; 6; 1 Participants
N/A N=168 Short Term Comparison of Two Different Techniques of Uterine Cesarean Incision Closure
Cesarean Section Complications
Primary: Cesarean Scar Defect in the Uterine Incisional Line — 12; 39 participants — p=0.0001
Phase 4 N=83 Prineo (Dermabond Protape) Versus Sutures for Full-thickness Surgical Incisions
Surgical Incisions
Primary: Continuous Apposition of the Skin Edges Without Wound Dehiscence or Re-closure as Measured by the Upper Limit of 95% Confidence Interval in Proportion of Successes for…
N/A N=40 ZIPS Study - Zip Incision aPproximation vs. Suture
Wound · Cardiac Arrhythmia
Primary: Overall Closure Time — 78; 216 seconds — p=<0.001
N/A N=168 Long Term Comparison of Two Different Techniques of Uterine Cesarean Incision Closure
Cesarean Section; Complications · Placenta Previa · Placenta Accreta
Primary: Placenta Previa — 18; 17; 0; 3 Participants
N/A N=86 Cleancision IntRaoperative Contamination prEvention Study
Wound Contamination · Colorectal Surgery
Primary: Efficacy (Enteric Bacterial Contamination on the Exposed Surface of the CleanCision Sheath Compared to the Protected Incision Edge) — 33.3; 9.5 % of participants with…
Phase 4 N=550 Subcuticular Suture for Cesarean Skin Incision Closure
Complications; Cesarean Section · Surgical Wound Infection
Primary: Number of Participants With Wound Complications (Surgical Site Infection (SSI), Hematoma, Separation, Seroma, Etc) — 23; 37; 16; 25 Participants — p=0.04
N/A N=37 Corneal Incisions With the IntraLase iFS Femtosecond Laser System
Cataract
Primary: Demonstration That the Femtosecond Laser Consistently Produces Desired Incisions. — 2.75; 2.74 mm
N/A N=298 Prevena™ Incisional Negative Pressure Wound Therapy in Re-operative Colorectal Surgery
Surgical Site Infection
Primary: Occurrence of Superficial Surgical Site Infection — 11; 21; 107; 128 Participants
N/A N=74 Randomized Controlled Trial of Subcuticular Skin Closure Versus Steri-strip S Closure
Breast Hypertrophy · Abdominal Elastosis · Breast Reconstruction
Primary: Scar Quality at 6 Months Postoperative — 3.8; 2.6 units on a scale
N/A N=109 Wound Infection Alexis Wound Retractor
Appendicitis
Primary: Post-operative Wound Infection, After Open Appendectomy — 1; 7 Participants
N/A N=92 The Use of the Prevena™ Incision Management System on Post-Surgical Cesarean Section Incisions
Post-operative Complications · Surgical Site Infection · Surgical Wound Infection
Primary: Incidence of Postoperative Surgical Site Occurrences (SSOs) up to Day 42 (+/- 10 Days) Post Cesarean Section Surgery. — 7; 2 participants
Phase 4 N=10 Use of Negative Pressure Wound Therapy in High Risk Surgical Closed Incisions
High Risk Abdominal Wounds
Primary: Number of Participants With Surgical Site Infections Within 1 Month (4 Weeks ) From Index Operation — 1 Participants
N/A N=151 A Skin Glue Versus Subcuticular Suture for Cesarean Closure Study
Cesarean Section · Complication · Wound
Primary: Patient Scar Satisfaction Scale Score — 13; 13.5 score on a scale
Phase 4 N=60 SURGX Antimicrobial Gel Versus Povidone-iodine Skin Incision Prep in Total Shoulder Arthroplasty
Surgery · Surgical Site Infection · Cutibacterium Acnes
Primary: Presence of Bacteria Within Shoulder Culture Using Incisional Prep vs. no Prep — 11; 9; 6 Participants — p=0.275
N/A N=105 Prevena™ vs Dermabond in Groin Wound Infections in Vascular Surgery
Wound Infection
Primary: Comparison of Healing of Groin Wounds Between Patients Treated With Prevena vs Dermabond — 41; 54 Participants
N/A N=278 Surgical Approach for Pilonidal Disease
Pilonidal Disease
Primary: Mobilization Time,Days — 3.21; 12.3 days
N/A N=94 The Use of a High-frequency Ultrasonic Knife in Breast Cancer Surgery
Breast Cancer
Primary: Drainage Volume — 182.6; 525.2 milliliters — p=<0.05
Phase 2 N=5 Study of GBT009 for Treatment of Incisional Wounds Following Breast Reconstruction Surgery
Scar Formation
Primary: Photography- Independent Scar Assessment Panel
N/A N=36 Force Modulating Tissue Bridges for Closure of Vertical Scars in Breast Reduction
Surgical Incision
Primary: Patient and Observer Scar Assessment Scale (POSAS)- Patient Scores 12M — 1.09; 1.22; 1.3; 1.87 score on a scale
Phase 3 N=583 Negative Pressure Wound Therapy in Post-Operative Incision Management
Negative-Pressure Wound Therapy
Primary: Number of Post-op Wound Complications — 2; 5; 42; 36 Wound Complications
N/A N=88 Surgical Site Infection With 0.05% Chlorhexidine (CHG) Compared to Triple Antibiotic Irrigation
Breast Cancer
Primary: Number of Participants With Surgical Site Infection — 7; 4 participants
Phase 2 N=165 Randomized Clinical Trial of Skin Closure With Staples Versus Suture
Wound Infection · Wound Complication
Primary: Number of Participants With Wound Disruption or Infection (Wound Complications) Occurring Within 4-8 Weeks of the Date of the Primary Surgery. — 28; 25 Participants