The use of tissue adhesive material to treat oral wounds.
Not Applicable
Completed
- Conditions
- Health Condition 1: K011- Impacted teeth
- Registration Number
- CTRI/2021/08/035768
- Lead Sponsor
- Self
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
1. All subjects 18 years and above with impacted mandibular third molar.
2. Subjects without known systemic disease such as Bleeding dyscrasia and immunosuppression (like Diabetes mellitus and AIDS).
3. Subjects not allergic to the drugs or anesthetic agent in the surgical protocol.
4. Subjects with good oral hygiene.
5. Subjects who were non-smokers
Exclusion Criteria
1.Subjects with any systemic diseases.
2.Pregnant or lactating.
3 With signs of pericoronitis or active infection.
4.With habits as smoking, and mouth breathing.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the wound closure ability and retentiveness of isoamyl-2-cyanoacrylate tissue adhesive in dentoalveolar surgical procedures. <br/ ><br>Timepoint: 7 days (post op day 1 to 7)
- Secondary Outcome Measures
Name Time Method To compare the wound healing outcome and post operative complications with the use of cyanoacrylate and conventional silksutures.Timepoint: Post op day1 to day 7