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Buccal Plate Augmentation With Different Hydroxyapatite Based Material

NCT01344577 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 96

Last updated 2017-02-23

No results posted yet for this study

Summary

The purposes of this study are : (first) to evaluate comparatively the effectiveness of 2 HA-based biomaterials when used for socket preservation with Buccal Plate Augmentation technique; (second) to evaluate clinical outcomes of socket preservation procedures performed using the Buccal Plate Augmentation technique.

Conditions

  • Edentulous

Sponsors & Collaborators

  • University of Ljubljana School of Medicine, Slovenia

    collaborator OTHER

  • University of Trieste

    lead OTHER

Principal Investigators

  • Claudio Stacchi, DDS · University of Trieste

  • Chiara O Navarra, DDS,PHD · University of Trieste

  • Roberto Di Lenarda, DDS, PHD · University of Trieste

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2013-12-31
Completion
2013-12-31

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01344577 on ClinicalTrials.gov