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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT00544323
Other study ID # cobiHMO
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 14, 2007
Last updated February 1, 2009
Start date November 2007

Study information

Verified date October 2007
Source Hadassah Medical Organization
Contact Lior Shapira, Prof.
Phone 972-2-6776183
Email shapiral@cc.huji.ac.il
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 25
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility 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

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
oral implant


Locations

Country Name City State
Israel Hadassah medical center, school of dentistry Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary radiographic changes in the alveolar bone height around the oral implant till 12 m post loading 12 months
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