Mandibular Ridge Splitting Versus Khoury Shell Technique

Horizontal Augmentation of Atrophic Posterior Mandible Clinical Trial

Official title:

Mandibular Ridge Splitting With Complete Separation of the Buccal Cortical Plate Versus Khoury Shell Technique for Horizontal Augmentation of Atrophic Posterior Mandible

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03781518
• Other study ID #: 290316
• Status: Completed
• Phase: N/A
• Start date: July 1, 2018
• Est. completion date: July 1, 2018

Study information

• Verified date: December 2018
• Source: Cairo University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Mandibular ridge splitting with complete separation of the buccal cortical plate versus Khoury shell technique for horizontal augmentation of atrophic posterior mandible

Recruitment information / eligibility

• Status: Completed
• Enrollment: 22
• Est. completion date: July 1, 2018
• Est. primary completion date: July 1, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 60 Years

Eligibility

Inclusion Criteria:

• Patients with atrophic mandible with residual bone width 3 to 4 mm.

• Both sexes.

• No intraoral soft and hard tissue pathology

• No systemic condition that contraindicate implant placement.

Exclusion Criteria:

• • Any pathology in the posterior mandible.

• Heavy smokers more than 20 cigarettes per day.

• Patients with systemic disease that may affect normal healing.

• Psychiatric problems

• Disorders to implant are related to history of radiation therapy to the head and neck neoplasia, or bone augmentation to implant site.

Related Conditions & MeSH terms

• Atrophy
• Horizontal Augmentation of Atrophic Posterior Mandible

Intervention

Procedure:
• ridge splitting in group and khoury shell technique in the other group
Mandibular ridge splitting with complete separation of the buccal cortical plate for horizontal augmentation of atrophic posterior mandible in one group and the other group will receive khoury shell technique by taking bone block from the ramus

Locations

Country	Name	City	State
Egypt	Cairo University	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Amount of horizontal bone gain (bone width)	measurement using CBCT	4 months
Secondary	Soft tissue healing	Dehiscence or no dehiscence	1 months