None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients aged 18 75 years. Systemically healthy individual. Patients requiring single tooth implant supported prosthesis. Adequate bone volume for implant placement without need for bone augmentation. Thin gingival mucosal phenotype with a peri-implant mucosal thickness of 2mm or less Patients willing to provide informed consent and comply with follow-up visits.
Exclusion criteria
Exclusion criteria: Smokers or tobacco users. Patients with uncontrolled systemic diseases e.g., uncontrolled diabetes, immunocompromised conditions. Patients having bleeding disorders or receiving anti-coagulant therapy. Pregnant or lactating women. History of radiation therapy in the head and neck region. Poor oral hygiene compliance. Sites requiring additional soft tissue grafting procedures. Patients on medications affecting wound healing (steroids, bisphosphonates).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate changes in peri-implant mucosal thickness and width of keratinized mucosa following conventional flap, pedicle flap, and T-PRF procedures during healing abutment placement.Timepoint: Baseline 1st week 2nd week 3rd week 4th week 3 months 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes include assessment of peri-implant clinical parameters, soft tissue healing, patient comfort, & esthetic outcomes following different soft tissue management techniques.Timepoint: Baseline 1st week 2nd week 3rd week 4th week 3 months 6 months | — |
Countries
India
Contacts
KALINGA INSTITUTE OF DENTAL SCIENCES