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Clinical Trials/ISRCTN92152389
ISRCTN92152389CompletedNot Applicable

A clinical feasibility study to evaluate the effectiveness and safety of VivescOs™ as bone graft for reconstruction of intra-oral osseous defects

IsoTis NV (The Netherlands)0 sites10 target enrollmentStarted: September 26, 2006Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
10

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Sex
All

Inclusion Criteria

  • Repair of the intra-oral defect was indicated as preparation for dental implant placement in a secondary stage.

Exclusion Criteria

  • 1. Presence of local or systemic disease;
  • 2. Pregnancy, cancertherapy;
  • 3. Previous participation in another trial within 30 days;
  • 4. Known hypersensitivity for penicillin, streptomycin.

Investigators

Sponsor
IsoTis NV (The Netherlands)

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