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Clinical Trials/NCT00137150
NCT00137150CompletedNot Applicable

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

University Hospital, Ghent2 sites in 1 country15 target enrollmentStarted: January 2005Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
15
Locations
2
Primary Endpoint
Implant survival at 6-12 months
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •18 years of age or older

Exclusion Criteria

  • •Medical risk patients

Outcomes

Primary Outcomes

Implant survival at 6-12 months

Secondary Outcomes

  • Prosthetic complications
  • Patient opinion

Investigators

Sponsor Class
Other

Study Sites (2)

Loading locations...

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Comparison of Outcome and Complications... | Clinical Trial