Health Condition 1: K055- Other periodontal diseases
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients in the age group 18 to 45 years from both genders without any blood disorder willing to undergo treatment with informed consent were included Sites with thin gingival phenotype gingival thickness less than 1 point 5mm in maxillary and mandibular canine and premolar region Plaque index PI less than 1 Gingival index GI less than 1 Bleeding on probing score of less than 10 percent will be included in the study
Exclusion criteria
Exclusion criteria: Patients undergoing active orthodontic treatment Taking any medication that may cause gingival enlargement Bruxism Any previous history of periodontitis or periodontal therapy Pregnant or lactating women Use of tobacco in any form Taking any blood thinners Patients under Aspirin medication Pre-existing mucogingival deformities
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim of the study is to compare and evaluate the efficacy of microneedling with the injectable platelet-rich fibrin versus microneedling with the concentrated platelet-rich fibrin in the management of the thin gingival phenotypeTimepoint: The outcome is assessed at baseline 3 months and 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)To assess the Gingival thickness following microneedling with i-PRF & microneedling with C-PRF in thin gingival phenotype. 2)To assess the Keratinized tissue width following microneedling with i-PRF & microneedling with C-PRF in thin gingival phenotype 3)To compare the Gingival thickness following microneedling with i-PRF & microneedling with C-PRF in thin gingival phenotype. 4)To compare the Keratinized tissue width following microneedling with i-PRF & microneedling with C-PRF in thin gingival phenotype.Timepoint: The outcome is assessed at baseline 3 months & 6 months | — |
Countries
India
Contacts
KVG Dental college and hospital