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NCT03669510 Clinical Trial

Assessment of the Neurosensory Alteration After Inferior Alveolar Nerve Lateralization

Implant Site Reaction Clinical Trial

Official title:
Assessment of the Neurosensory Alteration With Computer Guided Inferior Alveolar Nerve Lateralization Versus Non Guided Classic Technique

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03669510
Other study ID # 14422016552019
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2019
Est. completion date March 20, 2020

Study information
Verified date April 2024
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

: Assessment of the neurosensory alteration with computer guided inferior alveolar nerve lateralization versus non guided classic technique and measuring stability of implant after placement

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date March 20, 2020
Est. primary completion date March 20, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Adult patients with with atrophied posterior mandibular ridge - both sexes - NO intra oral soft and hard tissue pathology - NO systematic that contraindicate implant placement Exclusion Criteria: - Presence pathological lesion - Heavy smokers more than 20 cigarettes per day. - patients with systemic disease that may affect normal healing

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• computer guided IAN lateralization surgical technique
Tthe neurosensory alterations with computer guided inferior alveolar nerve lateralization versus non guided classic technique

Locations
Country Name City State
Egypt Faculty of Dentistry, Cairo University Cairo

Sponsors (1)
Lead Sponsor Collaborator
Mohamed Reda Mohamed Abdelhady

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Assessment of the neurosensory alteration- sensation over time subjective(a scale 1-10) assessing the sensation regaining over time subjective (a scale 1-10 ) 1 year
Secondary Implant stability Measurements of the implant stability immediately after placement by osstell At the placement and after exposure ( up to 6 months )
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