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OpenTrials
Completed

NCT Number: NCT00137150

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

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.

Completed

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Key information

Conditions

Dental Implants

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Ghent

Ghent, 9000, Belgium

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years of age or older

Exclusion criteria

  • Smoking
  • Medical risk patients

Treatment and study plan

Placement of implants

Procedure

Primary outcomes

  1. Implant survival at 6-12 months

Secondary outcomes

  1. Prosthetic complications

  2. Patient opinion

Sponsors and collaborators

Lead sponsor

University Hospital, Ghent

Other

Collaborators

  • Institut Straumann AG

Registry information

Important dates

Study start
2005
Study completion
2006
First posted
Aug 29, 2005
Registry last updated
Dec 28, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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