Clinical trials: Sutures
Bile Reflux
Omega Loop Gastric Bypass With And Without Anti-Reflux Sutures
This proposed trial is designed to answer the following questions: First, is biliary reflux to the distal esophagus present before OLGB and does it increase after the procedure? Second, does performing an OLGB with or without…
- Trial name
- NCT03097887
- Testing
- Omega Loop Gastric Bypass, Bilitec 2000™, V-Loc
- Where
- Austria
- Volunteers
- 100 people
- Sponsor
- Medical University of Vienna
Facial Lacerations
Cosmetic Outcomes and Patient Satisfaction After Facial Laceration Repair in the Emergency Department
Facial lacerations are commonly treated in the emergency department. The nature of the injury leads to a great deal of concern about the long-term cosmetic appearance of the wounds. Research Questions 1.
- Trial name
- NCT01514084
- Where
- United States
- Volunteers
- 160 people
- Sponsor
- Children's Hospitals and Clinics of Minnesota
Abdominal Obesity, Obesity
Suture Length Effects in Acupoint Implantation for Abdominal Obesity
Obesity is a metabolic disorder and has become a global health issue with a steadily increasing prevalence. According to the Health Promotion Administration's statistical report, the overweight and obesity rate among adults in…
- Trial name
- NCT07125716
- Testing
- 1 inch, 0.5 inch
- Where
- Taiwan
- Volunteers
- 78 people, healthy volunteers welcome
- Sponsor
- Chang Gung Memorial Hospital
Suture Related Complication
Timing of Suture Removal to Reduce Scarring in Skin Surgery
This is a single centre prospective randomized assessor blinded parallel group feasibility study that will be undertaken in the Royal Devon and Exeter Dermatology department.
- Trial name
- NCT05036785
- Testing
- Timing of suture removal
- Where
- United Kingdom
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Royal Devon and Exeter NHS Foundation Trust
Rotator Cuff Tears
Comparison of Outcomes of Rotator Cuff Repair With a Modified Versus Classic Double-Row Suture -Bridge Techniques
rotator cuff tears are one of the most common shoulder issues , affecting 20.7% of the general population .
- Trial name
- NCT06394856
- Testing
- Rotator Cuff Repair With a Modified Versus Classic Double-Row Suture -Bridge Techniques
- Where
- Egypt
- Volunteers
- 89 people
- Sponsor
- Sohag University
Osteoarthritis
Bandgrip vs Traditional Sutures TJA
Total Joint Arthroplasty (TJA) has become one of the most performed elective procedures. While the results of this procedure are often consistent with high patient satisfaction and return-to-function, wound-related complications…
- Trial name
- NCT05166642
- Testing
- Bandgrip Micro-Anchor Wound Closure, Suture closure
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- Center for Innovation and Research Organization
Diaphragmatic Eventration
Two Procedures for Uniportal Video Assisted Thoracoscopic Surgery to Treat Severe Cases of Diaphragmatic Eventration in Adult
highly elevated abnormal diaphragm is lowered to normal position by runuing suture accordion shaped or cut part of diphragm by stabler
- Trial name
- NCT07035366
- Testing
- stabled resection, running sutures
- Where
- 3 sites in Egypt
- Volunteers
- 30 people
- Sponsor
- Zagazig University
Ultra Tension-Reducing Suture Technique
A Self-Controlled Clinical Study of Fast-Absorbable Versus Slow-Absorbable Sutures Applied in Ultra Tension-Reducing Suture Technique
Hypertrophic scar formation after wound healing remains a clinical challenge in plastic surgery. Ultra Tension-Reducing Suture Technique is currently the primary surgical option for preventing and reducing hypertrophic…
- Trial name
- NCT07639372
- Testing
- Intervention 1: 5-0 Slow-absorbable PDS suture, Intervention 2: 5-0 Fast-absorbable Vicryl suture
- Where
- China
- Volunteers
- 20 people
- Sponsor
- Zhenzhen Zhang
Laceration of Skin, Injury Skin
Assessment of DAFILON® Suture Material for Skin Closure
In this non-interventional study (NIS) a polyamide non-absorbable suture (Dafilon®) will be evaluated for skin closure in adult and pediatric patients.
- Trial name
- SKINDA (NCT04617041)
- Where
- 2 sites in Germany, Spain
- Volunteers
- 115 people
- Sponsor
- Aesculap AG
Osteolysis
Incidence & Clinical Significance of Osteolysis Following PEEK Suture Anchor Use in Hand & Wrist Surgery
This prospective observational study evaluates the incidence \& clinical significance of osteolysis following polyetheretherketone (PEEK) suture anchor use in hand \& wrist surgery.
- Trial name
- NCT06824545
- Where
- United States
- Volunteers
- 180 people
- Sponsor
- University of Colorado, Denver
Suturing of Rectus Muscle at Cesarean Section
The Effect of Rectus Muscle Re-approximation at Cesarean Delivery on Postoperative Pain
The Effect of Rectus Muscle Re-approximation on Postoperative Pain Among Primigravida Singleton Pregnancies Who Underwent Elective Cesarean Section: A Randomized Prospective Trial.
- Trial name
- NCT05260970
- Testing
- Rectus muscle reapproximation at cesarean section
- Where
- Turkey (Türkiye)
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- Balikesir University
Carpal Tunnel Syndrome, Trigger Finger
Wound Closure Study in Carpal Tunnel and Trigger Finger Surgery
Does a difference in patient satisfaction and cosmetic outcome exist between wound closure with absorbable or non-absorbable sutures.
- Trial name
- NCT03781141
- Testing
- Wound closure
- Where
- United States
- Volunteers
- healthy volunteers welcome
- Sponsor
- Mayo Clinic
Hernia, Inguinal, Chronic Pain
Onstep Versus Lichtenstein, the Onli Trial.
The objective of this study is to evaluate chronic pain and sexual dysfunction after inguinal hernia repair involving mesh fixation with sutures (Lichtenstein) compared with no mesh fixation (Onstep).
- Trial name
- Onli (NCT01753219)
- Testing
- Onstep, Lichtenstein
- Where
- 4 sites in Denmark
- Volunteers
- 290 people
- Sponsor
- Jacob Rosenberg
Suture; Complications, Mechanical, Scar
Comparing 1 Week Versus 2 Week Cutaneous Suture Removal
Our goal is to compare the difference in surgical outcomes and patient satisfaction for surgical scars on the face between suture removal at 1 week versus 2 weeks.
- Conditions
- Suture; Complications, Mechanical, Scar, Surgery
- Trial name
- NCT05267002
- Testing
- Suture removal timing
- Where
- United States
- Volunteers
- 68 people, healthy volunteers welcome
- Sponsor
- DermSurgery Associates
Fusion of Spine
Comparative Analysis of Sutures for Fascial Closure in Spinal Surgery
STRATAFIX Symmetric PDS Plus sutures will reduce the time required for fascial closure following spinal surgery. A pilot study will aide in the design of a larger randomized controlled trial to compare suture closure time of the…
- Trial name
- NCT03533595
- Testing
- Barbed
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- Thomas Jefferson University
Isthmocele
Laparoscopic Isthmocele Repair
To evaluate postoperative outcomes in patients with isthmocele undergoing laparoscopic repair, comparing the efficacy of V-LocTM 180 and Polyglactin 910 Vicryl sutures.
- Trial name
- NCT06918275
- Testing
- Laparoscopic isthmocele repair using V-LocTM 180 barbed suture, Laparoscopic isthmocele repair using Polyglactin 910 vicryl suture
- Where
- Turkey (Türkiye)
- Volunteers
- 40 people
- Sponsor
- Kanuni Sultan Suleyman Training and Research Hospital
Inguinal Hernia, Inguinal Hernia Repair
Comparative Study of Inguinodynia After Inguinal Hernia Repair
To evaluate the postoperative pain and the relapse after the repair of the inguinal hernia by Lichtenstein technique with four different mesh types with different types of fixation in patients undergoing major ambulatory surgery.
- Conditions
- Inguinal Hernia, Inguinal Hernia Repair, Open Inguinal Hernia
- Trial name
- NCT03678272
- Testing
- HERNIOPLASTY WITH PANAVALE MESH, HERNIOPLASTY WITH PARIETEX PROGRIP MESH, HERNIOPLASTY WITH ADHESIX MESH
- Volunteers
- 270 people
- Sponsor
- Hospital General Universitario Elche
Pain, Acute, Laceration
Prospective Evaluation of Topical Analgesia for Laceration Repair in the Emergency Department
The purpose of this study is to determine if topical analgesia using a lidocaine and prilocaine cream improves pain scores compared to the usual local anesthesia using subcutaneous 1% lidocaine and adrenalin injected near the…
- Trial name
- NCT03071601
- Testing
- Lidocaine-Prilocaine Cream 2.5-2.5%, Lidocaine 1% Epinephrine 0.005mg/mL solution
- Where
- 2 sites in France
- Volunteers
- 132 people
- Sponsor
- Centre Hospitalier le Mans
Post Partum Hemorrhage
A Comparative Study Between Bakri Balloon and B Lynch Suture Used to Control Primary Postpartum Hemorrhage After Cesarean Section
Hundred (100) patients with primary postpartum hemorrhage during caesarean section due to atonic uterus will be recruited for this study.and randomized to either B lynch or Bakeri Ballon B-Lynch: A 70 mm round bodied hand needle…
- Trial name
- NCT03891082
- Testing
- B-Lynch, BALLOON INSERTION
- Volunteers
- 100 people
- Sponsor
- Cairo University
Continuous or Interrupted Suture
Analysis of Biliodigestive Anastomosis Techniques (BDA)
The aim of this prospective randomized controlled study is to determine the benefit-risk ratio (success rate, complication rate, tolerance) for patients with biliodigestive anastomosis by either continuous or interrupted suture.
- Trial name
- NCT02658643
- Testing
- Continuous suture technique, Interrupted suture technique
- Where
- Germany
- Volunteers
- 80 people
- Sponsor
- Technische Universität Dresden