Magnetic Mallet Versus Densah Bur for Crestal Sinus Left With Implant Placement in Maxilla (Randomized Controlled Clinical Trial)
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Maxillary Sinus Left
- Sponsor
- Hams Hamed Abdelrahman
- Enrollment
- 18
- Locations
- 1
- Primary Endpoint
- Change in pain socres
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
Background: Implant placement in the posterior maxilla is problematic procedure, not only due to inferior properties of bone but also due to loss of vertical bone height, which happens after extraction of posterior teeth. When the required additional height is few millimeters, indirect transcrestal sinus lifting is recommended. Aim: The aim of this study is to evaluate Densah bur versus Magnetic mallet in transcrestal sinus lifting procedure in edentulous molar and premolar maxillary region.
Investigators
Hams Hamed Abdelrahman
Assistant Lecturer of Dental Public Health and biostatistical consultanat
Alexandria University
Eligibility Criteria
Inclusion Criteria
- •Patient seeking replacement of missing maxillary posterior teeth by dental implant procedure.
- •Residual bone height is (5-7) mm measured from crestal bone to sinus floor.
- •Both genders.
- •Good general health;
- •Good oral hygiene.
Exclusion Criteria
- •Uncontrolled Diabetes.
- •Coagulation disorders.
- •Immunological disorders.
- •Previous radiation of the head and neck region.
- •Presence of chronic systemic diseases;
- •Presence of acute or chronic sinus problems;
- •Alcohol or drug abuse;
- •Heavy smokers.
Outcomes
Primary Outcomes
Change in pain socres
Time Frame: 3rd day, 1 week and 10 days
pain will be examined using visual analogue scale (VAS) 0 means no pain 10 means extreme pain
change in implant stability
Time Frame: baseline and 4 months
will be measured by the Resonance Frequency Analysis using osstel
Secondary Outcomes
- change in implant protrusion length(baseline and 4 months)
- change in bone density(baseline and 4 months)
- change in prescence of complications(3rd day, 1 week and 10 days)