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Extraction socket preservation procedure using platelet rich fibrin with and without calcium phosphate cement

Comparative evaluation of socket preservation procedure using platelet rich fibrin with and without calcium phosphate cementâ?? A Clinico-Radiographic Study.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/08/006100
Enrollment
15
Registered
2015-08-17
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

Health Condition 1: null- Systemically healthy patients between the age group 20-45 years having at least two non-molar teeth indicated for extraction.

Interventions

Intervention1: Calcium phosphate Cement: Calcium phosphate cement, dose-0.5cc Route-direct delivery to the extraction site assessment duration-6 months Control Intervention1: platelet rich fibrin: pla

Sponsors

Sinhgad Dental College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Systemically healthy patients between the age group 20- 45 years Patients having at least two non-molar teeth indicated for extraction. Indications for extraction include either root fracture, endodontic treatment failure, or non-restorable carious teeth. Alveolar sockets with 4 wall architecture. Patients willing to participate and sign an informed consent.

Exclusion criteria

Exclusion criteria: Patients who are systemically compromised. Patients having history of smoking or tobacco habit. Patients on medications that impair hematological parameter. Patient having history of bone disorder. Teeth having acute periapical or periodontal pathology. Pregnant and lactating females. Extraction sockets with one or more bony walls damaged.

Design outcomes

Primary

MeasureTime frame
Clinical and Radiographic of a. Marginal bone levels, calculated using a Williams periodontal probe as the distances between the coronal border of the stent and the mid-buccal and the mid-palatal aspect of the alveolar bone crest. b. The bucco-palatal width will be measured using a surgical caliper at mid-buccal and mid-palatal aspect of the socket at 1mm, 3mm and 5mm apical to the bone crest. Time point-at 6 monthsTimepoint: Time point-at 6 months

Secondary

MeasureTime frame
noneTimepoint: none

Countries

India

Contacts

Public ContactDr Nihal Devkar

Sinhgad Dental College and Hospital, Pune

shweta2747@gmail.com

Outcome results

None listed

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