Alveolar Bone Loss Around 3 Different Designs of Dental Implant: Prospective Comparative Clinical Trail
Primary Purpose
Alveolar Bone Loss
Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
oral implant
Sponsored by
About this trial
This is an interventional treatment trial for Alveolar Bone Loss focused on measuring alveolar bone, radiographic alveolar bone changes around oral implants of various designs 12 m post loading
Eligibility Criteria
Inclusion Criteria:
- healthy
- >18Y
- consent
- posterior mandibular missing teeth
Exclusion Criteria:
- chronic illness: diabetes, artheritis
- women: pregnancy, lactation
- non consent
- alcohol consumption
- smoking >10 p day
Sites / Locations
- Hadassah medical center, school of dentistry
Outcomes
Primary Outcome Measures
radiographic changes in the alveolar bone height around the oral implant till 12 m post loading
Secondary Outcome Measures
Full Information
NCT ID
NCT00544323
First Posted
October 14, 2007
Last Updated
February 1, 2009
Sponsor
Hadassah Medical Organization
1. Study Identification
Unique Protocol Identification Number
NCT00544323
Brief Title
Alveolar Bone Loss Around 3 Different Designs of Dental Implant: Prospective Comparative Clinical Trail
Official Title
Alveolar Bone Loss Around 3 Different Designs of Dental Implant: Prospective Comparative Clinical Trail
Study Type
Interventional
2. Study Status
Record Verification Date
October 2007
Overall Recruitment Status
Unknown status
Study Start Date
November 2007 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Hadassah Medical Organization
4. Oversight
5. Study Description
Brief Summary
comparison of alveolar bone resorbtion/ changes for a period of 12 month post loading of different designs and brands of oral implants. in this study, a comparison between straumann SLA-active implants to MIS Mistral and Mistral -X implants.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alveolar Bone Loss
Keywords
alveolar bone, radiographic alveolar bone changes around oral implants of various designs 12 m post loading
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Participant
Allocation
Randomized
Enrollment
25 (false)
8. Arms, Groups, and Interventions
Intervention Type
Device
Intervention Name(s)
oral implant
Primary Outcome Measure Information:
Title
radiographic changes in the alveolar bone height around the oral implant till 12 m post loading
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
healthy
>18Y
consent
posterior mandibular missing teeth
Exclusion Criteria:
chronic illness: diabetes, artheritis
women: pregnancy, lactation
non consent
alcohol consumption
smoking >10 p day
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lior Shapira, Prof.
Phone
972-2-6776183
Email
shapiral@cc.huji.ac.il
First Name & Middle Initial & Last Name or Official Title & Degree
Jacob Ekatein, Dr.
Phone
972-2-6776183
Email
drcobi@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lior Shapira Prof
Organizational Affiliation
Hadassah Medical Organization
Official's Role
Study Chair
Facility Information:
Facility Name
Hadassah medical center, school of dentistry
City
Jerusalem
Country
Israel
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lior Shapira, Prof
Phone
972-2-6776183
Email
shapiral@cc.huji.ac.il
First Name & Middle Initial & Last Name & Degree
Jacob Ekstein
12. IPD Sharing Statement
Learn more about this trial
Alveolar Bone Loss Around 3 Different Designs of Dental Implant: Prospective Comparative Clinical Trail
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