Clinical efficacy of indigenous Allograft
Not Applicable
- Conditions
- Health Condition 1: K068- Other specified disorders of gingiva and edentulous alveolar ridge
- Registration Number
- CTRI/2021/11/038030
- Lead Sponsor
- Aswin Kumar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Completely or partially edentulous patients planned for implant supported prosthesis, with inadequate bone dimensions for implant placement and require bone augmentation
Exclusion Criteria
Patients with acute rhinosinuitis, oroantral fistula.
Patient who had previously received bone graft on the site to be operated.
Tested positive for infection with HIV(by ELISA), Hepatitis B virus(HBsAg), Hepatitis C virus.
Patient taking intranasal medications.
Patients with uncontrolled systemic diseases (diabetes mellitus, hypertension).
Patients with autoimmune disorder, recent myocardian infraction.
Patient with bleeding or coagulation disorder.
Active malignancies, radiotherapy or chemotherapy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Histological - New bone formation, residual bone graft, Connective tissue contentTimepoint: 2 months post-operative
- Secondary Outcome Measures
Name Time Method Clinical healing, radiographic examinationTimepoint: 1 week, 4 weeks, 8 weeks