Oral and facial surgical incisions and traumatic lacerations
Conditions
Interventions
Closure of oral and facial surgical incisions and traumatic lacerations All investigators received standardized training in the use of Tisuacryl®. For patients with multiple eligible wounds, the trial
Sponsors
Center of Biomaterials of Havana University
Eligibility
Sex/Gender
All
Age
1 Years to 80 Years
Inclusion criteria
Inclusion criteria: 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.
Exclusion criteria
Exclusion criteria: 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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Dehiscence, immediately and 7-9 days. | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient Satisfaction, 7-9 days Physician Satisfaction, 7-9 days. Cosmetic appearance of the scar, 30 days | — |
Countries
Cuba
Contacts
Public ContactRosa Guerra Bretaña
Center of Biomaterials of Havana University
Outcome results
None listed