Tisuacryl® in Dentistry

Phase 3

Completed

• Conditions: Oral and facial surgical incisions and traumatic lacerations; Facial Injuries; Wounds and Injuries; Mouth; Face

• Registration Number: RPCEC00000044
• Lead Sponsor: Center of Biomaterials of Havana University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2008-09-12
• Last Update Posted: 2024-08-19

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 439

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

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified