Periimplantitis Clinical Trial
— GBROfficial title:
Preliminary Study of Hypro-Sorb® F Bilayer Bioabsorbable Membrane for Guided Tissue and Bone Regeneration
The main purpose of this study is to investigate the efficacy of Hypro-Sorb® F, a bilayered bioabsorbable membrane in inducing bone regeneration in different dental procedures requiring GBR.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | May 2009 |
Est. primary completion date | January 2008 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Cystectomy - Segmental growing of alveolar tissue - Lifting of the sinus bottom - Root amputation - Apicoectomy - Filling of the alveolus after resections in prosthetic surgical practice - Periimplantitis - Maxillofacial surgery Exclusion Criteria: - Inside bone fractures when acrylate adhesives are applied. |
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Israel | The Baruch Padeh Medical Center, Poriya | Tiberias |
Lead Sponsor | Collaborator |
---|---|
The Baruch Padeh Medical Center, Poriya |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | expected | 2 years | No |
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