NCT07394634

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

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at P25-P50 for not_applicable healthy

Timeline
8mo left

Started May 2025

Typical duration for not_applicable healthy

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress61%
May 2025Dec 2026

Study Start

First participant enrolled

May 1, 2025

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

January 23, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

February 6, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 30, 2026

Expected
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

February 6, 2026

Status Verified

January 1, 2026

Enrollment Period

1.2 years

First QC Date

January 23, 2026

Last Update Submit

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 INTERVENTION

Self healing in extraction socket

Autogenous tooth graft

EXPERIMENTAL

Autogenous tooth grafting in extraction socket

Procedure: autogenous tooth graft

Interventions

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

Autogenous tooth graft

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Faculty of Dentistrty

Jenjarum, Selangor, 42610, Malaysia

Location

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.

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

Locations