Evaluating Ribose Cross-linked Collagen Scaffold for Augmentation Buccal Contour at Dental-implant Sites: A Prospective Clinical Trial
Phase 1
- Conditions
- Single tooth edentulous space has facial bone thickness of at least 1 mm but no more than 2 mm and needs contouringRibose cross-linke dCollagen membrane, Buccal ridge contouring, biomarker analysis
- Registration Number
- TCTR20240809002
- Lead Sponsor
- C2F fund
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending (Not yet recruiting)
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
a.Adult patients with good general health or well-controlled disease (ASA Class I or II)
b.Edentulous area at anterior or posterior region of maxilla or mandible
c.Single tooth edentulous space has facial bone thickness of at least 1 mm and needs contouring
d.Implant with bone level approach
e.1 stage implant surgical protocol.
Exclusion Criteria
a.Patients who were unable to comply with the protocol requirements.
b.Patient has post-op dehiscence, infection.
c.Patients with a smoking habit (more than 10 cigarettes per day), alcoholism
d.Pregnant or lactating women
e.Patients who need adjacent implants.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method