None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients willing for voluntary participation and have signed informed consent for the described procedure 2) Patients having good physical and mental health and well formed or moderately formed residual alveolar ridge 3) Systemically healthy subjects (25-55 years) 4) Adequate bone quality and quantity at the implant site 5) Patients well motivated for implant therapy and maintaining good oral hygiene 6) Patients requiring bilateral implant placement
Exclusion criteria
Exclusion criteria: 1) Immunocompromised patients 2) Grafted site (previous or during implant placement)/ Immediate implant cases 3) Patients of chronic and aggressive periodontitis 4) Flapless procedures 5) Alcohol or drug abuse 6) Physiologically compromised patients 7) Patients with TMJ disorders , severe residual ridge resorption, orofacial tumors and gross facial deformity, mucositis, radiation therapy, parafunctional habits etc 8) Patients with active diseases of the implant bed (eg. Residual cysts)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The outcome of present study will help to determine the effectiveness of sodium hyaluronate in wound healing as well as bone density post implant placement.Timepoint: 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate effect of sodium hyaluronate on osseointegrationTimepoint: 6months | — |
Countries
India
Contacts
Atal bihari vajpayee university