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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04567966
Other study ID # PER 18-1D
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 28, 2018
Est. completion date March 3, 2020

Study information

Verified date September 2020
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Horizontal ridge augmentation using either cortical bone plate technique or cortico-cancellous block graft was the aim of the study. Bone quality was analyzed histomorphomterically, and horizontal dimensional changes were assessed using CBCT.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date March 3, 2020
Est. primary completion date January 6, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- Eligible patients aged 18 years or older with partial edentulism of the mandible

- The residual ridge width must be 4 mm or less

- Intra-oral donor sites should be available in the external oblique ridge and symphyseal area

Exclusion Criteria:

- Patients with general contraindications for implant surgery such as uncontrolled diabetes

- Irradiation of the head and neck region

- Intravenous bisphosphonate

- Pregnancy

- Smokers, alcoholics and drug abusers

Study Design


Related Conditions & MeSH terms

  • Atrophy
  • Horizontal Atrophy of Edentulous Alveolar Ridge

Intervention

Procedure:
Split-block technique
Horizontal ridge augmentation using the split-block technique where a cortical bone plate harvested from the external oblique ridge was split in half and fixed at a distance from the atrophied ridge. Then autogenous bone chips were packed in the gap between the plate and the ridge.
Cortico-cancellous block graft
Horizontal ridge augmentation using a cortico-cancellous block harvested from the chin of the mandible.

Locations

Country Name City State
Egypt Ain Shams University Cairo Abbassia

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of bone quality Histomorphometric analysis (Masson's Trichrome stain) 4 months
Secondary Horizontal ridge dimensional changes Measuring the linear horizontal changes using CBCT 4 months
See also
  Status Clinical Trial Phase
Recruiting NCT06221306 - Crestal Bone Loss Around Narrow Diameter Implants Versus Standard Diameter Implants With Bone Augmentation in Horizontally Deficient Posterior Mandibular Sites. N/A