Efficiency of Self Extracted Tooth Graft in Extraction Socket : A Clinical and Radiographic Study
Evaluating the Efficacy of Autogenous Tooth Graft (ATG) Material in Socket Preservation: A Clinical and Radiographic Study.
1 other identifier
interventional
20
1 country
1
Brief Summary
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).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable healthy
Started May 2025
Typical duration for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2025
CompletedFirst Submitted
Initial submission to the registry
January 23, 2026
CompletedFirst Posted
Study publicly available on registry
February 6, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
February 6, 2026
January 1, 2026
1.2 years
January 23, 2026
February 1, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Socket dimensional changes in autogenous tooth graft group and self healing group
Socket dimensional changes will be measure in clinical and radiographic measure Clinical measure: A stent will be made prior extraction and hole on the stent will be made to standardized measurement. Clinical measurement ( socket height) will be measure during post extraction, 1 month, 3 month and 6 month to observe the value of the resorption of the extraction socket . The discrepancy value is will be from ( 1month -baseline, 3month-baseline, 6month- baseline) Radiographic measure: CBCT will be taken post extraction 3 month and 6month. Socket width will be measure in 3mm below the socket and 5 mm below the socket. Other than that, mimic software will be used for the volumetric changes.
6 months
Secondary Outcomes (1)
Volumetric changes in autogenous tooth group and self healing group
6 months
Study Arms (2)
Self Healing Group
NO INTERVENTIONSelf healing in extraction socket
Autogenous tooth graft
EXPERIMENTALAutogenous tooth grafting in extraction socket
Interventions
Extracted tooth will be grind and processed into bone graft . This bone graft material will grafted into the extraction socket
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Mahsa Universitylead
Study Sites (1)
Faculty of Dentistrty
Jenjarum, Selangor, 42610, Malaysia
Related Publications (1)
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: 33565656RESULT
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr
Study Record Dates
First Submitted
January 23, 2026
First Posted
February 6, 2026
Study Start
May 1, 2025
Primary Completion (Estimated)
July 30, 2026
Study Completion (Estimated)
December 31, 2026
Last Updated
February 6, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share