Health Condition 1: K069- Disorder of gingiva and edentulousalveolar ridge, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants in the age range of 18 to 65 years Participants having good oral hygiene Presence of tooth or root piece indicated for extraction Participants willingness for implant placement
Exclusion criteria
Exclusion criteria: Any contraindication for surgery: Acute infection Medically compromised patients Uncooperative patients Non-compliant patients for oral hygiene maintenance Subjects with abnormal bleeding/clotting time Presence of any pathology causing facial bony plate dehiscence History of Irradiation in Head and Neck Uncontrolled diabetic patients (reported levels of glycemia over the normal threshold) Current pregnancy or lactation Current Smokers
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Maximum Bucco-lingual width of the socket at the time of socket preservation and at the time of implant placement will be measured using ridge measuring pliers clinically and radiographically with CBCT. 2.Pain Scores using VAS scale within 24 hours after extraction and socket preservation in both the groups. 3.Bone mineral density will be evaluated after four months of socket preservation radiographically by CBCT. 4.Primary implant stability will be evaluated at the time of implant placement by insertion torque value (ITV) 5.Clinical signs of inflammation (bleeding on probing, plaque index, gingivitis index, probing pocket depth and percussion test) after six months of implant placement will be recorded in both the groups. 6.Radiographic analysis evaluating peri-implant bone loss at six months post-implant placement in both the groups. Timepoint: Baseline and four months | — |
Secondary
| Measure | Time frame |
|---|---|
| nilTimepoint: nil | — |
Countries
India
Contacts
V.Y.W.S. Dental College and Hopital, Amravati