se of tissue adhesive Tisuacryl® in the closure of oral and facial wounds

Center of Biomaterials of Havana University0 个研究点目标入组 439 人开始时间: 2008年9月12日最近更新: 2024年8月19日

适应症

试验速览

暂无简介。

研究类型: Interventional
分配方式: N/a: Single Arm Study. Masking: Open. Control Group: Placebo. Assignment: Single Group. Purpose: Treatment

•Adult patients up to 80 years old who consent to participate in the clinical trial Children more than 1 year old whose parents or tutors consent to participate in the clinical trial Patients who fulfill the established diagnostic criteria: 1) Non deep facial skin wounds that do not required subcutaneous suture; less than 3 cm in length and 0,5 cm in width. 2) Non deep oral wounds that do not required subcutaneous sutures; less than 5 cm in length and 0,5 cm in width.

•Patients with wounds contaminated by foreign body Patients with wounds that require debridement Patients with crushing and puncture wounds or those produced by bites or scratches of animals or humans Patients with wounds in an area of important skin tension Patients with radiation therapy. Patients with mental incapacity and/or severe psychological disorders Pregnant and breastfeeding women Patients that do not consent to participate in the study

发起方

Center of Biomaterials of Havana University