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Saving the bone after tooth removal

Comparative evaluation ofVolumetric bone dimensional changesin extraction sockets preserved with Calcium Phosphosilicate bone substitutes with and without platelet rich fibrin. â?? A randomized controlled clinical trial - ARP

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/09/021024
Enrollment
30
Registered
2019-09-02
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Socket preservation: Compliant patients were scheduled for surgical therapy. Before the start of surgical therapy, extraction sites will be randomly assigned for the designed treatment
forGroup II ( Test ), residual sockets will be filledwith Calcium Phosphosilicate and forGroup III ( Test ), residual sockets will be filled with Calcium Phosphosilicate mixed with platelet rich fibri

Sponsors

Dr PSG Prakash
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: (1) Patients with age rangeof 19 â?? 55years. (2) Patients not contraindicated for periodontal surgeries. (3) Residual extraction sockets possessing intact bone in all dimensions. ( 4- walled bony defect ) (4) Tooth included for extraction with caries, trauma andendodontic complications (Root fracture). (5) Need for implant restoration at the site of extraction. (6) Patient who have given written and verbal informed consent.

Exclusion criteria

Exclusion criteria: (1) Presence of periodontitis on the tooth to be extracted; (2)Chronic therapy under non-steroidal anti-inflammatory drugs, Bisphosphonates and Corticosteroids; (3) Current smokers( >10 cigarettes per day); (4) Plaque index >30%; (5) Evidence of loss of the buccal bone wall during tooth extraction; and (6) Pregnancy

Design outcomes

Primary

MeasureTime frame
Horizontal and vertical measurements assessed at 6 months with CBCT. Bone density measurents in Hounsfield units at 6 months with CBCT. Timepoint: Horizontal and vertical measurements assessed at 6 months with CBCT. Bone density measurents in Hounsfield units at 6 months with CBCT.

Secondary

MeasureTime frame
To assess Pain, discomfort, swelling and Interference with daily activitiesusing 10 cm Visual analogue scale at 1 week post operativelyTimepoint: 1 week later

Countries

India

Contacts

Public ContactDr PSG Prakash

Srm dental college

akashpsg@gmail.com9840870990

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026