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Immediate Implant With no Graft , Autogenous Graft or Xenograft.

Immediate Implant Placement in Maxillary Esthetic Zone Without Augmenting the Jumping Gap Versus the Use of Autogenous Bone Particulates or Demineralized Bovine Bone Graft (Randomized Clinical Trial)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03851224
Enrollment
30
Registered
2019-02-22
Start date
2018-09-01
Completion date
2019-11-01
Last updated
2019-02-22

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

Conditions

Dental Diseases

Brief summary

Immediate implant placement with no graft , autogenous graft or xenograft with provisionalization.

Detailed description

Immediate implant placement in maxillary esthetic zone without augmenting the jumping gap versus the use of autogenous bone particulates or demineralized bovine bone graft (Randomized Clinical Trial)

Interventions

PROCEDUREcontrol group

immediate implant with immediate loading using no graft

PROCEDUREstudy group

immediate implant with immediate loading using autogenous bone graft

PROCEDUREstudy group 2

immediate implant with immediate loading using (Geistlich Bio-Oss®) xenograft

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Masking description

Immediate implant placement in maxillary esthetic zone without augmenting the jumping gap versus the use of autogenous bone particulates or demineralized bovine bone graft.

Intervention model description

Immediate implant placement in maxillary esthetic zone without augmenting the jumping gap versus the use of autogenous bone particulates or demineralized bovine bone graft.

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* patients with non-restorable teeth

Exclusion criteria

* intra oral pathology and systemic conditions that contraindicate dental implants.

Design outcomes

Primary

MeasureTime frameDescription
evaliuation of labial bone changes6 monthEvaluation the thickness of the facial bony wall by millimeter in the CBCT
evaluation of marginal bone changes6 monthsevaluation of interproximal bone changes by millimeter in the CBCT

Secondary

MeasureTime frameDescription
pink aesthetic score6 monthevaluation of soft tissue changes surround implant by pink aesthetic score

Countries

Egypt

Contacts

Primary ContactMostafa M Attiea, B.S.D
mosattiea3110@gmail.com00201009080414
Backup ContactMostafa M Attiea, B.S.D
ahmed.zayed@dentistry.cu.edu.eg0021009080414

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026