Use of an Oxidized Regenerated Cellulose After Thyroid Surgery: A Prospective, Randomized Study
NCT01171079 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL
Last updated 2010-07-28
Summary
The purpose of this study is to evaluate the effects and safety of oxidized, regenerated cellulose as an absorbable adhesion barrier after thyroidectomy.
Conditions
- Thyroidectomy
Interventions
- DEVICE
-
application of oxidized regenerated cellulose
Sponsors & Collaborators
-
Seoul National University Hospital
lead OTHER
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
Countries
- South Korea
Study Locations
More Related Trials
-
Preoperative Silicone Ointment and Wound Healing
NCT05461157 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Evaluation of the Benefit of the Use of Autologous Glue Prepared With RegenKit®-Surgery Device in Abdominoplasty
NCT02930447 ·Status: UNKNOWN ·Phase: NA
-
A Comparison of 2-octyl Cyanoacrylate Skin Adhesive and Polyester Mesh for Wound Closure in Total Knee Arthroplasty, A Randomized Controlled Study
NCT06232018 ·Status: COMPLETED ·Phase: NA
-
Efficacy and Safety of 0.25% Timolol Gel in Healing Surgical Open Wounds
NCT03452072 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Efficacy and Safety of the Investigational Device, SurgiShield Anti-Adhesion Barrier Gel
NCT01895933 ·Status: COMPLETED ·Phase: NA
-
Aesthetic Outcome of Layered Closure vs. Layered Closure Followed by 2-Octyl Cyanoacrylate
NCT05449457 ·Status: COMPLETED ·Phase: NA
-
Force Modulating Tissue Bridges for Closure of Vertical Scars in Breast Reduction
NCT05028816 ·Status: COMPLETED ·Phase: NA
-
A Comparative Efficacy and Safety Study Between Two Silver Containing Dressings In Post-Op Wound Healing
NCT01605968 ·Status: TERMINATED ·Phase: NA
-
Evaluation of Opticell Ag on Split-Thickness Skin Graft Donor Sites in Adult Subjects
NCT02642679 ·Status: COMPLETED ·Phase: NA
-
The SERI® Surgical Scaffold Use in Reconstruction Post Market Study for Tissue Support and Repair in Breast Reconstruction Surgery
NCT01256502 ·Status: COMPLETED ·Phase: NA
-
Recolonization Following Preoperative Disinfection Plastic Adhesive Drapes
NCT01316588 ·Status: COMPLETED ·Phase: PHASE3
-
Case Series Assessing TissuGlu® Surgical Adhesive in Flap Surgery for Decubitus Repair
NCT03482999 ·Status: COMPLETED
-
Activated Carbon Interphase Effect on Surgical Incisions vs.Two Common Wound Dressings
NCT04038671 ·Status: WITHDRAWN ·Phase: NA
-
Prineo (Dermabond Protape) Versus Sutures for Full-thickness Surgical Incisions
NCT00557947 ·Status: COMPLETED ·Phase: PHASE4
-
An Investigator-blind Multi-center Prospective Study for the Efficacy and Safety of Silicon Gel (Dermatix)
NCT01004536 ·Status: UNKNOWN ·Phase: PHASE4
-
Efficacy of a Fibrin Sealant in Burn Surgery
NCT00181974 ·Status: COMPLETED ·Phase: NA
-
Silicone Taping for the Improvement of Abdominal Donor Site Scars
NCT04506255 ·Status: RECRUITING ·Phase: NA
-
Safety and Efficacy Study of Fibrin Sealant Grifols as an Adjunct to Hemostasis During Peripheral Vascular Surgery
NCT01662856 ·Status: COMPLETED ·Phase: PHASE3
-
Silicone Gel Versus Onion Extract Gel as Prevention for Postsurgical Scars
NCT01861119 ·Status: COMPLETED ·Phase: PHASE3
-
Evaluation of Cohera TissuGlu in the Management of Wound Drainage Following Abdominoplasty
NCT01331798 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Incisional Negative Pressure Wound Therapy for Preoperatively Irradiated Lower Extremity Soft Tissue Sarcoma Wounds
NCT02638298 ·Status: COMPLETED ·Phase: NA
-
Effect of Transparent, Self-drying Silicone Gel on the Treatment of Hypertrophic Abdominal Scars
NCT01078428 ·Status: COMPLETED ·Phase: PHASE4
-
Prevention of Hypertrophic Scars or Keloids
NCT00849004 ·Status: UNKNOWN ·Phase: NA
-
Fibrin Sealant in Eyelid Surgery
NCT05358977 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
Suture Repair of Lacerations in the ED: Comparison Between Two Suture Materials
NCT05281666 ·Status: TERMINATED ·Phase: NA