NCT06773104

Brief Summary

24 patienta with non restorable anterior teeth underwent extraction with immediate implant installation using bone grafts either autogenous tooth bone graft or allogenic bone graft Autogenous tooth bone graft group (study group): 12 patients will have immediate implant placement with autogenous tooth bone graft. • Allogeneic bone graft group (control group): 12 patients will have immediate implant placement with allogeneic bone graft (demineralized freeze dried bone allograft - cortico cancellous).

Trial Health

87
On Track

Trial Health Score

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

Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2024

Geographic Reach
1 country

1 active site

Status
completed

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 Start

First participant enrolled

March 25, 2024

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

December 30, 2024

Completed
15 days until next milestone

First Posted

Study publicly available on registry

January 14, 2025

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 16, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 16, 2025

Completed
Last Updated

January 20, 2026

Status Verified

January 1, 2026

Enrollment Period

1.6 years

First QC Date

December 30, 2024

Last Update Submit

January 16, 2026

Conditions

Keywords

autogenous tooth bone graftallogenic bone graftgrafting the jumbing gapimmediate dental implant

Outcome Measures

Primary Outcomes (2)

  • labial bone thickness

    measuring thickness of labial bone labial to the implant

    6 months

  • marginal bone loss

    6 months

Secondary Outcomes (3)

  • bone density around dental implant

    6 months

  • implant secondary stability

    6 months

  • implant success

    6 months

Study Arms (2)

Autogenous tooth bone graft group

EXPERIMENTAL

Twelve patients receiving immediate implant placement with autogenous fresh partially demineralized dentin graft.

Procedure: Allogeneic bone graft with immediate implant placement

Allogeneic bone graft group (control group)

ACTIVE COMPARATOR

Patients receiving immediate dental implant placement with allogeneic bone graft (DFDBA) for grafting of the jumping gap.

Procedure: immediate implant with allogenic bone graft

Interventions

after atraumatic extraction immediate implant will be inserted with allogenic bone graft

Allogeneic bone graft group (control group)

Immediate dental implant placement with grafting of the jumping gap using allogeneic bone graft (DFDBA).

Autogenous tooth bone graft group

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Patients with non restorable maxillary anterior teeth need to be extracted.
  • Thin labial plate of bone of the tooth to be extracted.
  • Patients age above 20years old.
  • Good oral hygiene.
  • No signs of acute infection or inflammation

You may not qualify if:

  • Prior radiation therapy.
  • Soft and hard tissue pathology at the operation site.
  • Any relevant systemic disease or medication that might compromise bone healing.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Dentistry

Tanta, 3111, Egypt

Location

Study Officials

  • diab abdelgaied diab, master

    faculty of dentistry tanta university

    PRINCIPAL INVESTIGATOR
  • Rafic ramadan bedir, professor

    faculty of dentistry tanta university

    PRINCIPAL INVESTIGATOR
  • Ibrahim mohammed nowair, professor

    faculty of dentistry tanta university

    PRINCIPAL INVESTIGATOR
  • Mona samy sheta, lecturer

    faculty of dentistry tanta university

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: non restorable anterior teeth with thin labial plate of bone
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal investigator

Study Record Dates

First Submitted

December 30, 2024

First Posted

January 14, 2025

Study Start

March 25, 2024

Primary Completion

October 16, 2025

Study Completion

October 16, 2025

Last Updated

January 20, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations