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Enrolling by invitation NCT07394634

Efficiency of Self Extracted Tooth Graft in Extraction Socket : A Clinical and Radiographic Study

No phase Interventional Healthy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: autogenous tooth graft.
Who it may be relevant to
Registry conditions: Healthy. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Malaysia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Evaluating the Efficacy of Autogenous Tooth Graft (ATG) Material in Socket Preservation: A Clinical and Radiographic Study.

Overview

This is the clinical trial. The goal of this clinical trial is to test whether self extracted tooth graft (autogenous tooth graft ) able to preserved the extraction socket effectively. Our aim is to answer is there any difference in dimensional changes in extraction socket in clinically and radiographically Researchers will compare autogenous tooth graft with self-healing extraction socket in radiographic and clinical measurement. Participant will be randomly allocated into 2 groups ( Test or controlled group) Test group will be autogenous tooth grafting post extraction. After removed any caries, calculus and any gilling material, the extracted tooth will be grind with grinder and processed using BONMAKER machine. (which the bone graft is washed with hydrogen peroxide, hydrogen chloride and alcohol isopropyl) and controlled group will be self healing group. Both group will withdraw 20cc blood for PRF ( Plasma rich fibrin) membrane and place into the socket and secured with suture. They will be reviewed post extraction 1 week ( to ensure there is no infection ) , 2 week ( for suture removal ) , 1 months ( For clinical measurement) , 3 months (For clinical and radiographic measurement) and 6 months (For radiographic measurement).

Interventions

  • Procedure autogenous tooth graft
    Extracted tooth will be grind and processed into bone graft . This bone graft material will grafted into the extraction socket

Primary outcome measures

  • Socket dimensional changes in autogenous tooth graft group and self healing group [Time frame: 6 months]
Secondary outcome measures (1)
  • Volumetric changes in autogenous tooth group and self healing group [Time frame: 6 months]

Eligibility criteria

Inclusion criteria

  • Age> or equal to 18 years old
  • Presence of adjacent teeth to the extraction site
  • Healthy ,or well controlled systemic disease
  • Lower and upper incisors, lower premolar/ first molar
  • Full mouth plaque score < 15%
  • Adequate space for a dental implant restoration \*Patient with previous diagnosis of periodontitis will be required to have a successfully completed course of periodontal treatment before enrolment.

Exclusion criteria

  • Smokers and vapers
  • Acute infection or sinus tract in relation to the tooth that require extraction
  • Pregnant or lactating women
  • Patient received antibiotic for past 1 month
  • Loss of more than 50% buccal or lingual /palatal bone at the time of extraction
  • Patient on medication that altered bone metabolism or bone healing such as bisphosphonates, chemotherapeutic drugs or immunosuppressive agents

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Malaysia · 1 center
  • Faculty of Dentistrty — Jenjarum

Publications

  • Elfana A, El-Kholy S, Saleh HA, Fawzy El-Sayed K. Alveolar ridge preservation using autogenous whole-tooth versus demineralized dentin grafts: A randomized controlled clinical trial. Clin Oral Implants Res. 2021 May;32(5):539-548. doi: 10.1111/clr.13722. Epub 2021 Mar 1. PMID 33565656

Identifiers

NCT: NCT07394634 · RMC/JANUARY/2025/EC07

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗