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A clinical trial to evaluate the effectiveness of autogenous tooth graft for socket preservation

A randomised prospective clinical trial for evaluation of clinical effectiveness of autogenous tooth graft in socket preservation which is a clinical,radiological and histological study. - ATG

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064825
Enrollment
10
Registered
2024-03-27
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

None listed

Interventions

Intervention1: To evaluate the clinical , radiological and histological effectiveness of autogenous tooth graft in preserving the extracted alveolar socket: To assess the effectiveness of autogenous t

Sponsors

Tanya Singh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age between 20 and 50 years. Systemically healthy patients.ASA 1,ASA 2 Patients who require tooth extraction due to localized periodontitis,trauma and tooth fracture. Patient having a tooth indicated for extraction which could be used for autograft. Patient who received instruction on the purpose of the clinical study and gave his /her consent.

Exclusion criteria

Exclusion criteria: Systemic illness such as diabetes mellitus, cardiac diseases, immune-compromised , patients taking medications such as corticosteroids, calcium channel blocker or bisphosphonates which are known to interfere with the outcome. Pregnant and lactating patients. Grossly decayed and RCT treated teeth Alcoholics and Smokers. Patients who demonstrate poor oral hygiene maintenance. Patient who has received radiation therapy. Patient who has acute infections.

Design outcomes

Primary

MeasureTime frame
1.To assess the effectiveness of autogenous tooth graft in preserving the extracted alveolar socket , using radiological segmental CBCT evaluation of socket width and socket height and histological evaluation using punch biopsy after 6 months. Timepoint: 6 months

Secondary

MeasureTime frame
To prepare the site for future prosthetic rehabilitation and implant placementTimepoint: 6 months

Countries

India

Contacts

Public ContactDrK David Tyro

Army college of dental sciences

navaljeetkaurmann@gmail.com9876911090

Outcome results

None listed

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