Trial Of Resorbable versus Non-Resorbable sutures for traumatic lacerations of the face (TORN Face)

Cambridge University Hospitals NHS Foundation Trust0 个研究点目标入组 200 人开始时间: 2021年3月16日最近更新: 2023年10月23日

适应症

试验速览

暂无简介。

•1. Wounds with the following characteristics:
•1.1. Significant contamination or presenting later than 12 h after the initial injury
•1.2. Animal or human bites
•1.3. Wounds requiring antibiotic prophylaxis
•1.4. Wounds amenable to closure with adhesive tape or tissue adhesive
•1.5. Complex lacerations requiring closure under general anaesthetic
•1.6. Not amenable to primary closure (significant tissue loss requiring more complex closure methods)
•1.7. Lacerations involving cartilage or bony injuries
•1.8. Injuries involving parotid gland, parotid duct, or facial nerve
•1.9. Wounds requiring smaller than 5/0 suture material
•2. Scalp lacerations due to difficulties in assessing the cosmetic outcome
•3. Presence of accompanying injury/polytrauma requiring more extensive medical/surgical intervention as a priority
•4. History of:
•4.1. History of keloid or hypertrophic scar formation
•4.2. Collagen vascular disorders
•4.3. Prolonged corticosteroid use
•4.4. Type I diabetes or poorly controlled type II diabetes
•4.5. Primary or secondary immunodeficiency (including systemic chemotherapy)
•4.6. Clotting or bleeding disorders
•4.7. Allergy to chloramphenicol 1% ointment
•4.8. Recent radiotherapy to the head and neck
•5. Unable to give written informed consent, including patients considered under the influence of alcohol (or recreational/medicinal substances) at the time of patient consultation

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