Clinical trials: Sutures
Wound Healing Cosmetic Result
Clinical Study Into the Cosmetic Results of Leukosan Adhesive
This clinical study aims to assess whether the benefits of using Leukosan Adhesive on trocar incisions are greater or equivalent to those provided by the standard therapy of transcutaneous sutures.
- Trial name
- NCT02179723
- Testing
- Leukosan Adhesive, Transcutaneous suture
- Where
- Germany
- Volunteers
- 77 people
- Sponsor
- Dr. Stephanie Krause
Sport Surgery
Sport Surgery Products Outcomes - A Post-market Follow-up
Teknimed is currently conducting a post-market clinical follow-up which will confirm performance, safety and usability for all the Teknimed range of Sports products.
- Trial name
- NCT06532929
- Testing
- Orthopaedic surgeries (ankle), Orthopaedic surgeries (shoulder), Orthopaedic surgeries (knee)
- Where
- 10 sites in France
- Volunteers
- 390 people
- Sponsor
- Teknimed
Wound Closure
Symmetric on Total Knee Arthroplasty (TKA)
A post-marketing prospective, multicenter, randomized controlled study to evaluate the wound closure efficiency of STRATAFIX™ Symmetric PDS™ Plus Knotless Tissue Control Device (STRATAFIX Symmetric PDS Plus) compared to…
- Trial name
- SFX (NCT03305887)
- Testing
- "STRATAFIX™ Symmetric" Knotless Tissue, VICRYL® PLUS, "STRATAFIX Spiral" sutures
- Where
- 7 sites in China
- Volunteers
- 184 people
- Sponsor
- Johnson & Johnson Medical, China
Use of the Vloc Suture, Elevation of the Mid-face
Use of V-Loc Suture for Mid-face Lifting in Short-flap Rhytidectomy
This study will evaluate and measure the Vloc suture's ability to elevate the mid-face when using a short flap, short incision technique in during a traditional face-lift.
- Trial name
- NCT02023307
- Testing
- V-Loc Suture
- Where
- United States
- Volunteers
- 15 people, healthy volunteers welcome
- Sponsor
- Lifestyle Lift
Adiposity
Study on the Performance of Symmcora® Mid-term Suture Versus Novosyn® Suture in Patients Undergoing Robotic Assisted Gastric Bypass Surgery
The study is designed as a prospective, mono-centric, randomized, patient blinded comparison of unidirectional barbed suture (Symmcora® mid term, UBS) vs. a conventional suture (Novosyn®, CS).
- Trial name
- BARGASTRO (NCT05433688)
- Testing
- Robotic assisted gastric bypass surgery
- Where
- Germany
- Volunteers
- 150 people
- Sponsor
- Aesculap AG
Pathological Processes in the Posterior Fossa, Dura Defects
Fibrin Sealant for the Sealing of Dura Sutures
The purpose of this study is to investigate the efficacy and safety of FS VH S/D 500 s-apr, a double virus-inactivated biological two-component fibrin sealant, for use in posterior fossa surgery as an adjunct to dura and dura…
- Trial name
- NCT00681824
- Testing
- Fibrin Sealant, Vapor Heated, Solvent/Detergent-treated with 500 IU/mL thrombin and synthetic aprotinin (FS VH S/D 500 s-apr), Standard of care
- Where
- 13 sites in United States, Canada
- Volunteers
- 95 people
- Sponsor
- Baxter Healthcare Corporation
Rotator Cuff Repairs
PMCF Study on the Safety, Performance and Clinical Benefits Data of the ComposiTCP
The study is a multicenter, retrospective and prospective, non-randomized, noncontrolled, and consecutive series post-market study.
- Trial name
- NCT07080450
- Where
- France
- Volunteers
- 43 people
- Sponsor
- Zimmer Biomet
Eye Diseases
Dafilon® Suture Material in Patients Undergoing Ophthalmic Surgery
This is an observational, retrospective postmarket clinical follow-up study and includes all patients who underwent any ophthalmic surgery using Dafilon® suture in the selected centres between 2018 and 2020, therefore no sample…
- Trial name
- OPHTHADA (NCT05968443)
- Testing
- ophthalmic surgery
- Where
- Malaysia
- Volunteers
- 200 people
- Sponsor
- Aesculap AG
Meniscal Tears
Evaluation on Safety and Effectiveness of the An All-inside, All-suture Meniscal Repair Device
This study is a prospective, multi-center, randomized controlled pre-market clinical trial in China to evaluate the safety and efficacy of the JuggerStitch™ Meniscal Repair Device for arthroscopic meniscal repair.
- Trial name
- NCT06899659
- Testing
- JuggerStitch™ Meniscal Repair Device, Fast-Fix 360 Meniscal Repair System
- Where
- 2 sites in China
- Volunteers
- 94 people
- Sponsor
- Zimmer Biomet
Episiotomy, Perineal Tear
A Study Comparing Topical Skin Adhesive or Sutures for Closure Due to Episiotomy or Perineal Tears Following Childbirth
This is a randomized controlled trial and multi-centered study with a 2-arm design. The treatment group will receive topical skin adhesive for skin closure of their wound and the control will receive sutures.
- Trial name
- NCT00196508
- Testing
- High Viscosity DERMABOND
- Where
- 5 sites in United States
- Volunteers
- 118 people
- Sponsor
- Ethicon, Inc.
Injury of Abdominal Wall
Effect of Stitch Technique on the Occurrence of Incisional Hernia After Abdominal Wall Closure
The major long term complication of abdominal wall closure after a median laparotomy is the development of an incisional hernia.
- Trial name
- ESTOIH (NCT01965249)
- Testing
- Long stitch, Short Stitch
- Where
- 9 sites in Austria, Germany
- Volunteers
- 425 people
- Sponsor
- Aesculap AG
Episiotomy
PMCF-study Using Novosyn® Quick Suture Material for Perineal Repair After Episiotomy
The aim of this study is to show that the performance of Novosyn® Quick suture material is comparable with other suture material used for episiotomy.
- Trial name
- EPINOQ (NCT02762357)
- Testing
- Novosyn® Quick
- Where
- 2 sites in Spain
- Volunteers
- 46 people
- Sponsor
- Aesculap AG
Laparotomy, Incisional Hernia
Clinical Performance and Safety of Suture-TOOL
The goal of this single arm intervention study is to investigate the safety and performance of a suturing device for closure of the midline incision after open abdominal surgery.
- Conditions
- Laparotomy, Incisional Hernia, Wound Infection, Closure Technique
- Trial name
- NCT05695157
- Testing
- Suture-TOOL
- Where
- Sweden
- Volunteers
- 38 people
- Sponsor
- Suturion AB
Vascular Closure, Femoral Arteriotomy Closure
The Ladera Large Bore Closure Feasibility Study
This study evaluates the safety and performance of the Ladera Medical suture-mediated large bore closure (LBC) system in gaining post procedure hemostasis in subjects undergoing interventional catheterization procedures using a…
- Trial name
- NCT06358157
- Testing
- Ladera LBC System
- Where
- 3 sites in Australia
- Volunteers
- 30 people
- Sponsor
- Ladera Medical
Prostate Cancer
Symmcora® Long-term Bidirectional Barbed Suture for Anastomosis in Patients Undergoing Robot Assisted Radical Prostatectomy
The aim of this observational study is to show the superiority of the bidirectional barbed suture (Symmcora® Longterm) in terms of time to perform the vesicourethral anastomosis after robot assisted radical prostatectomy compared…
- Trial name
- BARVANA LONG (NCT06055946)
- Testing
- robotic assisted radical prostatectomy
- Where
- 2 sites in Spain
- Volunteers
- 70 people
- Sponsor
- Aesculap AG
Weight Loss
OverStitch NXT Endoscopic Suture System
To demonstrate the safety and efficacy of OverStitch NXT Endoscopic Suture System for endoscopic sleeve gastroplasty（ESG） in obese populations to support the registration of OverStitch NXT for ESG indication.
- Trial name
- NCT07276815
- Testing
- OverStitch NXT Endoscopic Suture System
- Where
- China
- Volunteers
- 136 people
- Sponsor
- Boston Scientific Corporation
Rotator Cuff Tears, Rotator Cuff Injuries
PMCF Study on the Safety, Performance and Clinical Benefits Data of the Quattro X Broadband
The study is a multicenter, retrospective and prospective, non-randomized, noncontrolled, and consecutive series post-market study.
- Trial name
- NCT05690776
- Where
- 2 sites in France
- Volunteers
- 106 people
- Sponsor
- Zimmer Biomet
Laceration of Skin
A Post-Market Study of BandGrip in Traumatic Wound Closure Compared to Suture
an unbalanced (2:1) randomized study comparing two methods of traumatic skin closure in an ER setting: BandGrip vs suture
- Trial name
- NCT03628690
- Testing
- BandGrip, Suture
- Where
- United States
- Volunteers
- 45 people
- Sponsor
- BandGrip
Skin Closure
PMCF-study Using Novosyn® Quick Suture Material for Skin Closure
The aim of this study is to show that the performance of Novosyn® Quick suture material is comparable with other suture material used for skin closure.
- Trial name
- SKINNOQ (NCT02680886)
- Testing
- Novosyn® Quick
- Where
- 2 sites in France, Germany
- Volunteers
- 100 people
- Sponsor
- Aesculap AG
Gastrointestinal Diseases, Laparotomy
Clinical Use of an Absorbable Coated Suture Material in Surgery (Safil)
The purpose is to test a coated polyglycolic acid multifilament suture in gastrointestinal surgery as part of a controlled randomized single blinded parallel group trial.
- Conditions
- Gastrointestinal Diseases, Laparotomy, Anastomosis, Surgical, Absorbable, Coated Sutures
- Trial name
- NCT00645684
- Testing
- Gastrointestinal Anastomosis
- Where
- 3 sites in Hungary
- Volunteers
- 210 people
- Sponsor
- Aesculap AG