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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04075942
Other study ID # PER 6-3-1
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 2021
Est. completion date January 2021

Study information

Verified date January 2021
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Using customized Xenograft bone shell with mixture of autogenous and xenograft particulate in modified cortical shell technique. by 3D printed model from The CT scans segmentation by special software


Description:

Using customized Xenograft bone shell by 3D printed model from The CT scans segmentation by special software ( Mimics ) . All surgeries were performed by the same surgeon . All surgical procedures were performed under strict aseptic conditions, all patients received infiltration local anesthesia (Articaine 4% 1:100 000 epinephrine). a midcrestal incision was made in the anterior region using No. 15 blade. A full thickness mucoperiosteal flap was raised to expose the underlying alveolar ridge. The residual remaining bone in the area was minimal, with a maximum measured ridge thickness of 3 or 4 mm. 'To reconstruct the lost alveolar bone, an xenograft bone shell approximately 1 to 2 mm thick was shaped, after 3D print the bone shell were fixed to the buccal defect, using screws . 'The space between the plate and the existing palatal bone wall was then filled using a combination of autograft bone chips and xenograft bone particles . Periosteal releasing incision is done to obtain stress free primary closure. The flap will then be closed using interrupted 4/0 resorbable sutures. After 4 month will insert implant . After 3 month will insert final restoration which will be mostly PMF .


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 8
Est. completion date January 2021
Est. primary completion date January 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 15 Years to 70 Years
Eligibility Inclusion Criteria: - patients with atrophic Anterior Maxillary Ridges Exclusion Criteria: - Heavy smokers - Uncontrolled diabetic patients. - Pregnant patients. Psychiatric patient - pathology related to bone.

Study Design


Related Conditions & MeSH terms

  • Atrophic Anterior Maxillary Ridges
  • Atrophy

Intervention

Procedure:
Atrophic Anterior Maxillary Ridges
Use of modified cortical shell technique grafted with customized Xenograft bone shell

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Manal Ahmed Hassan Ahmed

Outcome

Type Measure Description Time frame Safety issue
Primary Bucco-lingual bone width gain. 4 months