Health Condition 1: K069- Disorder of gingiva and edentulousalveolar ridge, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: POSTMENOPAUSAL FEMALE PATIENTS WHO ARE COOPERATIVE AND MOTIVATED FOR DENTAL IMPLANT TREATMENT. FEMALE PATIENTS WITH ADEQUATE BONE VOLUME.GOOD GENERALIZED PERIODONTAL HEALTH. FEMALE PATIENTS WILLING TO FOLLOW THE STUDY PROTOCOL. FEMALE PATIENTS WILLING TO MAINTAIN GOOD ORAL HYGIENE AFTER DENTAL IMPLANT PLACEMENT.
Exclusion criteria
Exclusion criteria: FEMALE PATIENTS WITH ANY SYSTEMIC DISEASES. FEMALE PATIENTS HAVING ADVERSE HABITS TOBACCO USE OR SMOKING ALCOHOL. PREGNANT AND LACTATING PATIENTS. PATIENTS HAVING ALLERGY TO THE MATERIALS TO BE USED DURING OPERATION. PATIENTS HAVING SEVERE BRUXISM OR CLENCHING. PATIENT ON IMMUNOSUPPRESSED OR IMMUNOCOMPROMISED DRUGS.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| THE STUDY IS EXPECTED TO DEMONSTRATE IMPROVED GINGIVAL THICKNESS AND PERI IMPLANT SOFT TISSUE IN SITES TREATED WITH MICRONEEDLING AND IPRF. IT MAY VALIDATE A MINIMALLY INVASIVE ALTERNATIVE TO SURGICAL SOFT TISSUE AUGMENTATION.Timepoint: 6 MONTHS | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
SURENDERA DENTAL COLLEGE AND RESEARCH INSTITUTE