Clinical and Radiographic Assessment of Socket Preservation Using Autogenous Demineralized Dentin Matrix Versus Xenograft

Clinical and Radiographic Assessment of Socket Preservation Using Autogenous Demineralized Dentin Matrix Versus Xenograft: A Randomized Controlled Trial

Status

Completed

Phases

Unknown

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT07777588

Enrollment

Registered

2026-08-20

Start date

2025-06-28

Completion date

2026-04-22

Last updated

2026-08-20

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

Conditions

Autogenous Demineralized Dentin, Xenograft Bone Graft

Brief summary

Total of 40 participants were planned for enrollment for socket preservation, 20 in the Autogenous Demineralized Dentin group and 20 in the Xenograft group these materials used for socket preservation after extraction. Participants were assessed for changes in bucco-lingual width at different point, bone density and changes in bone volume, keratinized tissue width.

Interventions

PROCEDUREAutogenous Demineralized Dentin

application of Autogenous Demineralized Dentin

PROCEDUREapplication of xenograft

application of xenograftxenograft

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender

ALL

Age

18 Years to 50 Years

Healthy volunteers

Yes

Inclusion criteria

premolar indicated for extraction

Exclusion criteria

smokers , condition affecting bone metabolism

Design outcomes

Primary

Measure	Time frame	Description
bucco-lingual bone width	6 months	measuring width in mm at different points

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 21, 2026