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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00137150
Other study ID # 2004/420
Secondary ID
Status Completed
Phase N/A
First received August 26, 2005
Last updated December 19, 2007
Start date January 2005
Est. completion date September 2006

Study information

Verified date December 2007
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study is a comparison of outcome and complications encountered in flapless surgery and immediate loading versus the classical surgical approach and loading after 6-8 weeks in the posterior maxilla.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date September 2006
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years of age or older

Exclusion Criteria:

- Smoking

- Medical risk patients

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Placement of implants


Locations

Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (2)

Lead Sponsor Collaborator
University Hospital, Ghent Institut Straumann AG

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Implant survival at 6-12 months
Secondary Prosthetic complications
Secondary Patient opinion
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