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

Completed

• Conditions: Intra-oral bone defects, loss of teeth/molars; Musculoskeletal Diseases

• Registration Number: ISRCTN92152389
• Lead Sponsor: IsoTis NV (The Netherlands)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2006-09-26
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 10

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.

Study & Design

• Study Type: Interventional
• Study Design: Not specified