Cutaneous Use of Tisuacryl®
- Conditions
- Wounds and InjuriesSurgical and traumatic wonds
- Registration Number
- RPCEC00000046
- Lead Sponsor
- Center of Biomaterials of Havana University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 674
Patients of both genders, between 1 and 80 years old. Adult patients who gave the informed consent. Children whose parents or tutors signed the informed consent. Patients who fulfill the established diagnostic criteria:: 1)Surgical incisions less than 6 cm long which had subcutaneous sutures. Longer incisions could be considered using anchor sutures every 3-4 cm. 2)Recent (under 6 hours) non deep cutaneous lacerations (that do not require internal suture) less than 4 cm long and 0.5 cm in width.
Patients with wounds contaminated by any foreign body Patients with wounds produced by bites or scratch of animals or humans, puncture or crushing Patients with wounds located in an area of high skin tension Patients with mental incapacity and/or severe psychological disorders Pregnant and breastfeeding women Patients that do not consent to participate in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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