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OpenTrials
Completed

NCT Number: NCT00286533

Evaluation of Implants Placed in the Regular Dentist's Practice

This study is an evaluation of the implants placed in a regular dentist's practice regarding:

* gingiva condition * stability of implant * prothetic quality * questionnaires for the patients

Completed

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Key information

Conditions

Dental Implant

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

  • Patients with implants placed in a regular dentist's practice

Treatment and study plan

Clinical examination (implant stability, gingiva condition, etc.)

Procedure

Clinical examination (implant stability, gingiva condition, etc.) to follow

Questionnaires

Procedure

Questionnaires are used.

Primary outcomes

  1. gingiva condition

    Time frame: t0

Other outcomes

  1. stability of implant

    Time frame: t0

  2. prothetic quality

    Time frame: t0

  3. questionnaires for the patients

    Time frame: t0

Sponsors and collaborators

Lead sponsor

University Hospital, Ghent

Other

Registry information

Official study title

Retrospective Evaluation of Implants Placed in the Regular Dentist's Practice. A Study to Evaluate Implant Success, Prosthetic Complications, Opinion of the Patient, and Quality of Care

Important dates

Study start
2006
Primary completion
2008
Study completion
2008
First posted
Feb 3, 2006
Registry last updated
Dec 21, 2022

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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