A clinical trial to study effect of bio-glue in patients for the closure of wounds following oral surgery.
Phase 4
Completed
- Conditions
- Health Condition 1: K053- Chronic periodontitisHealth Condition 2: K069- Disorder of gingiva and edentulousalveolar ridge, unspecifiedHealth Condition 3: K011- Impacted teethHealth Condition 4: K136- Irritative hyperplasia of oral mucosaHealth Condition 5: K116- Mucocele of salivary glandHealth Condition 6: K041- Necrosis of pulp
- Registration Number
- CTRI/2022/12/048035
- Lead Sponsor
- Dr Kanishk Srivastava
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
1.Patient with the age 18 years and above will be selected for the study.
2.Minor oral surgical procedures were closure of intra oral surgical incisions are required
3.Procedures like, multiple extractions, canine exposure, transalveolar extractions, surgical extraction of impacted third molars and canine, alveoloplasty, biopsy, and excision of mucocele are included in the study.
4.Clean incisions which can be approximated without tension are included.
5.Patient who agreed to follow the study protocol.
Exclusion Criteria
Patients will not be considered for the study with the following criteria:
1.Immunocompromised patients.
2.Uncontrolled diabetes
3.Bleeding disorders
4.Uncooperative patients
5.Neurological disorders
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improved and early wound healing of test siteTimepoint: 1 week
- Secondary Outcome Measures
Name Time Method Efficacy of tissue adhesive for early wound healing of the surgical site, healing will be much better and patients compliance will be more towards the product under investigation.Timepoint: 3rd and 7th day post op.