Clinical trials: Suture
Rotator Cuff Tears
Cutting-through at the Greater Tuberosity
The investigators evaluated the correlation between cutting-through at the greater tuberosity (GT) just medial to the lateral knotless anchor in arthroscopic suture-bridge rotator cuff repair and the bone mineral density (BMD) of…
- Trial name
- NCT04587180
- Testing
- Arthroscopic suture-bridge rotator cuff repair
- Volunteers
- 95 people
- Sponsor
- Chuncheon Sacred Heart Hospital
Mitral Valve Regurgitation, Mitral Valve Prolapse
CE Mark Study for the Harpoon Medical Device in Poland
The purpose of this study is to evaluate the safety and performance of the Harpoon Medical TSD-5. The Harpoon device will provide many significant advantages over current surgical interventions including: 1) a small minimally…
- Conditions
- Mitral Valve Regurgitation, Mitral Valve Prolapse, Mitral Valve Insufficiency
- Trial name
- NCT02432196
- Testing
- Harpoon Medical Device
- Where
- 2 sites in Poland
- Volunteers
- 26 people
- Sponsor
- Edwards Lifesciences
Obesity
ULTIMATE Study for Weight Loss
The purpose of this study is to help find out more about how the Primary Obesity Surgery Endoluminal (POSE) procedure makes patients feel less hungry and fuller faster, leading to weight loss.
- Trial name
- ULTIMATE (NCT01771276)
- Testing
- g-Cath Suture Anchor Delivery Catheter
- Where
- Spain
- Volunteers
- 10 people
- Sponsor
- USGI Medical
DNS
Trans-septal Quilting Suturing vs Intranasal Silicone Splinting in Septoplasty
There is currently little data comparing intranasal silicone splinting versus trans-septal quilted suturing in terms of preventing problems following septoplasty.
- Trial name
- NCT07537920
- Testing
- trans-septal quilting suturing, intranasal silicone splinting
- Where
- Pakistan
- Volunteers
- 60 people
- Sponsor
- Shahida Islam Medical Complex
Volar Plate Injury
Mini-anchor Versus Pull-out Suture for Surgical Management
Volar plate injuries of the joint are among the most common traumatic lesions in the hand. These injuries result from hyperextension trauma, leading to volar plate avulsion, often accompanied by collateral ligament injuries or…
- Trial name
- NCT07209605
- Testing
- Group A Pull-out Suture Technique, Group B- Mini-anchor Technique
- Volunteers
- 12 people
- Sponsor
- Sohag University
Quality of Life
Three Dimensional Evaluation of Nasolabial Changes Following Classic vs Without Alar Base Suture After Le Fort I Osteotomy
Three dimensional evaluation of nasolabial changes following classic vs without alar base suture after Le Fort I osteotomy A randomized controlled clinical trial
- Trial name
- NCT04021836
- Testing
- 3d evaluation of nasolabial change
- Volunteers
- 20 people
- Sponsor
- Cairo University
Cesarean Section; Infection
Subcuticular Skin Closure at Cesarean Delivery
Subcuticular skin closure with suture after cesarean has been shown to result in lower rates of wound complications than with staple closure.
- Trial name
- NCT03536832
- Testing
- Cesarean Section with Vicryl, Cesarean Section with Prolen
- Where
- Turkey (Türkiye)
- Volunteers
- 220 people, healthy volunteers welcome
- Sponsor
- Kanuni Sultan Suleyman Training and Research Hospital
Regional Anesthesia, Sciatic Nerve Block
Comparing Through-the-Needle With Suture-Method Catheter Designs for Popliteal Nerve Blocks
Following painful surgical procedures, postoperative analgesia is often provided with a single-injection peripheral nerve block.
- Trial name
- NCT03442036
- Testing
- Suture-Method Technique, Through-the-Needle Technique
- Where
- United States
- Volunteers
- 70 people, healthy volunteers welcome
- Sponsor
- University of California, San Diego
Skin Closure of Surgical Incisions by Tissue Glue vs Suture
Tissue Glue (Cyanoacrylate) Versus Conventional Suture in Kidney Donors
By means of a prospective, randomised trial the investigators want to examine skin closure in living donors - subjected to laparoscopic, hand-assisted nephrectomy - by tissue glue (Cyanoacrylate (Liquiband)) versus conventional…
- Trial name
- TG-CYANO (NCT01521871)
- Testing
- Skin wound closure by tissue glue, Skin wound closure by conventional suture + dressing
- Where
- Norway
- Volunteers
- 64 people
- Sponsor
- Oslo University Hospital
Parturition, Delivery, Obstetric
Randomized Controlled Trial of the Effectiveness of Perineal Pain and Security of the Suture Led by the Result of Hemostasis Versus Manual Compression Routine Suture Perineal Tears of First Degree During Childbirth
During childbirth, the recommendations have evolved to a restriction of episiotomy. This reduction results in an increase of superficial vaginal and perineal tears.
- Trial name
- ImSOLENCE (NCT02870712)
- Testing
- Suture of perineum, hemostatis by digital compression
- Where
- France
- Volunteers
- 112 people, healthy volunteers welcome
- Sponsor
- Centre Hospitalier Universitaire de Besancon
Bariatric Surgery Candidate, Obesity, Morbid
Suture Reinforcement to Reduce the Leak Rate After Sleeve Gastrectomy
Staple line reinforcement (SLR) has been suggested as a mean of reducing the risk of sleeve leakage or bleeding. The aim of this study is to analyze if the suture reinforcement can be used to reduce the leakage rate after sleeve…
- Conditions
- Bariatric Surgery Candidate, Obesity, Morbid, Leak, Anastomotic, Bleeding
- Trial name
- NCT05987787
- Testing
- laparoscopic sleeve gastrectomy without suture reinforcement, laparoscopic sleeve gastrectomy with suture reinforcement
- Where
- Italy
- Volunteers
- 33 people
- Sponsor
- University of Foggia
Shoulder Pain, Shoulder Injuries
MDR SureLock All-Suture Anchor
To report the outcomes of a series of patients with recurrent anterior and/or posterior shoulder instability who underwent surgical repair of the affected labrum using the SureLock all-suture anchor.
- Conditions
- Shoulder Pain, Shoulder Injuries, Shoulder Disease, Shoulder Pain Chronic
- Trial name
- NCT04093700
- Testing
- SureLock All-Suture Anchor
- Where
- United States
- Volunteers
- 24 people
- Sponsor
- Zimmer Biomet
Cesarean Section
Trial Comparing Barbed and Non-barbed Suture for Uterine Incision Closure at Cesarean Section
This was an unblinded randomized controlled trial. Women were randomized to uterine closure with the knotless barbed suture (Stratafix PDS, Ethicon) or Vicryl (Ethicon) at the time of elective cesarean.
- Trial name
- barbed (NCT02962011)
- Testing
- Knotless barbed suture, polyglactin 910
- Where
- Israel
- Volunteers
- 102 people
- Sponsor
- Ziv Hospital
Hernia
TEP Versus Open Minimal Suture Repair for the Sportsman's Groin
Sportsman's hernia is defined as a weakness or disruption of the posterior wall of the inguinal canal. Open hernia repair with or without mesh or laparoscopic techniques with mesh have been advocated in the treatment of…
- Trial name
- SPORT (NCT02297711)
- Testing
- Total ExtraPeritoneal, Open minimal suture repair
- Where
- United Kingdom
- Volunteers
- 65 people
- Sponsor
- Manchester University NHS Foundation Trust
Phoniatric Evaluation of Total Thyroidectomy
Phoniatric Evaluation and Comparison of Patients Who Underwent Sutureless Thyroidectomy With Vessel Closure Devices and Conventional Total Thyroidectomy With Suture
The purpose of this study is to compare effect of sutureless thyroidectomy with vessel closure devices and conventional thyroidectomy with suturing on voice quality with phoniatric evaluation.
- Trial name
- NCT01865006
- Where
- Turkey (Türkiye)
- Volunteers
- 90 people
- Sponsor
- Istanbul University
Rotator Cuff Injury
Suture Anchor Comparison in Rotator Cuff Repairs
Patients will be randomized to receive HEALICOIL™ REGENESORB (the study anchor) or TWINFIX Ultra HA, a similar comparative product, for use in the repair of their shoulder injury.
- Trial name
- NCT02350647
- Testing
- Suture Anchor HEALOCOIL, Suture anchor Twinfix Ultra HA
- Where
- United States
- Volunteers
- 64 people
- Sponsor
- The Hawkins Foundation
Cesarean Scar Defect (Isthmococele)
Incision-Parallel Double-Layer Non-Locking Versus Single-Layer Locked Uterine Closure After Primary Caesarean Delivery: A Randomized Controlled Trial
This randomized controlled trial was conducted to compare two uterine closure techniques in women undergoing primary cesarean delivery.
- Trial name
- NCT07841028
- Testing
- Single-Layer Locked Uterine Closure, Double-Layer Incision-Parallel Nonlocking Uterine Closure
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people
- Sponsor
- Onur Karaaslan
Cesarean Scar Defect; Transvaginal Diverticulum Resection
Cesarean Section Defect Mechanism and Transvaginal Repair
Background and aims: Cesarean section defect (CSD) can cause abnormal uterine bleeding or impaired fertility, which severely impaire the quality of life in women of pregnant age.
- Trial name
- NCT05643703
- Testing
- Suture method
- Volunteers
- 300 people
- Sponsor
- Peking Union Medical College Hospital
Zone 2 Flexor Tendon Lacerations of the Hand
The Effects of a Stainless Steel Suture MGH Flexor Tendon Repair Coupled With Early Aggressive Range of Motion Rehabilitation: a Randomized Controlled Trial
The investigators are comparing the combination of a stainless steel repair and aggressive early active range of motion rehabilitation protocol for flexor tendon lacerations in the hand with a current, accepted treatment offered…
- Trial name
- NCT01344980
- Testing
- Stainless steel suture, Polypropylene suture, Aggressive early active range of motion rehabilitation
- Where
- Canada
- Volunteers
- 24 people, healthy volunteers welcome
- Sponsor
- University of Manitoba
Obesity
Safety and Feasibility of an Endoluminal-suturing Device (Endomina TM) for Gastric Reduction
Objectives: Study to evaluate safety and feasibility of an endoluminal vertical gastroplasty (EVG) using an endoluminal-suturing device.
- Trial name
- NCT02534662
- Testing
- ENDOMINA
- Where
- Belgium
- Volunteers
- 11 people, healthy volunteers welcome
- Sponsor
- Theodor Bilharz Research Institute