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Enrolling by invitationNCT07604142CAD-CAMUpdated May 22, 2026

Allogenic Bone Block for Oro-Antral Communication Closure for Subsequent Implant Placement

An interventional study of Extraction will be performed atraumatically using a piezotome surgical motor with an extraction kit in Tooth Loss, sponsored by Tanta University. Enrolling by invitation at 1 site in Egypt. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2026-05-22.

Sponsored by Tanta University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
13
Allocation
Not applicable
Ages
20 Years and older
Sex
All
01

Study summary

13 patients will be included in this study with a badly destructed upper molar indicated for extraction. Cone beam computerized tomography images revealed the presence of a large bone defect associated with oro-antral communication with the maxillary sinus. after extraction, The prefabricated allogenic scaffold will be seated. then 6 months later, implant will be inserted.

Read the detailed description

13 patients will be included in this study with a badly destructed upper molar indicated for extraction. Cone beam computerized tomography images revealed the presence of a large bone defect associated with oro-antral communication with the maxillary sinus. : Extraction will be performed atraumatically using a piezotome surgical motor with an extraction kit. After removal of tooth, oro-antral communication will be verified .The prefabricated CAD-CAM allogenic bone will be seated and covered with nonporous d-PTFE membrane which was secured with simple interrupted sutures. After 6 months, a new CBCT scan will be performed. A mucoperiosteal flap will be reflected ,and a bone biopsy will be taken using a trephine bur. Under strictly aseptic circumstances, the selected implant will be inserted

02

Conditions studied

  • Tooth Loss

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Keywords

  • CAD-CAM allogenic block
  • oroantral communication
  • radiographic analysis
  • histological analysis
03

Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • ≥ 20 badly destructed upper molar indicated for extraction CBCT revealed the presence of a large bone defect associated with oro-antral communication with the maxillary sinus

Exclusion criteria

Exclusion Criteria:

  • any systemic disesse affect healing heavy smoker sinus disease
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
13 participants (estimated)

Study arms

  • Experimental
    a badly destructed upper molar indicated for extraction. Cone beam computerized tomography images re

    a badly destructed upper molar indicated for extraction. Cone beam computerized tomography images revealed the presence of a large bone defect associated with oro-antral communication with the maxillary sinus. Extraction will be performed atraumatically using a piezotome surgical motor with an extraction kit. After removal of tooth, oro-antral communication will be verified .The prefabricated scaffold will be seated and covered with nonporous d-PTFE membrane. after 6 months, a bone biopsy will be taken using a trephine bur. Under strictly aseptic circumstances, the selected implant will be inserted.

    Device: Extraction will be performed atraumatically using a piezotome surgical motor with an extraction kit

Interventions

  • DeviceExtraction will be performed atraumatically using a piezotome surgical motor with an extraction kit

    Extraction will be performed atraumatically using a piezotome surgical motor with an extraction kit. After removal of tooth, oro-antral communication will be verified .The prefabricated CAD-CAM Allogenic bone will be seated and covered with nonporous d-PTFE membrane

05

What researchers measure

Primary outcomes

  1. the integration of graft

    CBCT

    Time frame: 6 months

  2. histological analysis of graft

    histomorphometric analysis

    Time frame: 6 months

06

Study locations

1 site
  • Faculty of Dentistry
    Tanta, 3111, Egypt
07

Registry details

Key details

Study ID
NCT07604142
Lead sponsor
Tanta University
Responsible party
mona samy sheta (lecturer, Tanta University) — Principal investigator
First posted
May 22, 2026
Start date
Sep 20, 2025
Primary completion
Oct 25, 2026 (estimated)
Completion
Nov 30, 2026 (estimated)
Last update
May 22, 2026

Study contacts

mohamed helal, lecturer
principal investigator · Tanta University
rehab ghouraba, professor
principal investigator · Tanta University
aya alsherif, lecturer
principal investigator · Tanta University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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