Immediate Implant Placement With Provisionalization Using Different Bone Grafts as a Space Filling Material in the Maxillary Esthetic Zone

NCT03741036 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2018-11-19

No results posted yet for this study

Summary

compare autogenous bone graft, xenograft and nanohydroxyapatite in immediate implant w placement in maxillary esthetic zone with provisionalization

Conditions

  • Dental Implant Failed

Interventions

PROCEDURE

Autogenous bone graft as space filling in immidiate implant placment

* The selected patients will be informed of the nature of the research work and informed consent will be obtained (immediate implant placement grafting with autogenous bone graft) * Patients will be subjected to CBCT (diagnostic for upper arch). * Local anesthesia will be given to the patient. * Scrubbing and draping of the patient will be carried out in a standard fashion for intra oral procedures. * The procedure will be carried out flapless. * In the study group: Atraumatic extraction * The extraction socket will be evaluated for absence of any fenestration or granulation tissues

PROCEDURE

Deprotinized bovien as space filling in immidate implant placement

* The selected patients will be informed of the nature of the research work and informed consent will be obtained (immediate implant placement grafting with deprotinized bovien material) * Patients will be subjected to CBCT (diagnostic for upper arch). * Local anesthesia will be given to the patient. * Scrubbing and draping of the patient will be carried out in a standard fashion for intra oral procedures. * The procedure will be carried out flapless. * In the study group: Atraumatic extraction * The extraction socket will be evaluated for absence of any fenestration or granulation tissues

PROCEDURE

Nano-hydroxiapatite alloplast in immidiate implant placement

* The selected patients will be informed of the nature of the research work and informed consent will be obtained (immediate implant placement grafting with nano-hydroxiapatite alloplast material ) * Patients will be subjected to CBCT (diagnostic for upper arch). * Local anesthesia will be given to the patient. * Scrubbing and draping of the patient will be carried out in a standard fashion for intra oral procedures. * The procedure will be carried out flapless. * In the study group: Atraumatic extraction * The extraction socket will be evaluated for absence of any fenestration or granulation tissues

Sponsors & Collaborators

  • Cairo University

    collaborator OTHER
  • Mohamed tarek mohamed youssif omar

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-11-27
Primary Completion
2019-07-27
Completion
2019-08-17

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03741036 on ClinicalTrials.gov