clinical study of individually made high strength ceramic and individually made high performance polymer connection between artificial tooth and artificial root for single-tooth replacement.
Phase 4
- Conditions
- Health Condition 1: null- Healthy patients coming to the dept for replacement of single tooth with implant crown willing to participate in the study.Health Condition 2: K084- Partial loss of teeth
- Registration Number
- CTRI/2017/08/009385
- Lead Sponsor
- self
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Healthy Patients requiring implant supported prosthesis, willing to participate in the study.
2.Cases with sufficient Osseo integration of implant.
3.Cases of single tooth restorations in maxillary anterior and premolar region.
Exclusion Criteria
1.Pregnant ladies.
2.Persons who develops any systemic diseases during the follow up period.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Survival rate, Peri-implant soft tissue health,Bone level, and Difference colour of final restoration and peri-implant mucosa.Timepoint: Base line, 6 months, 12 months, 24 months
- Secondary Outcome Measures
Name Time Method ilTimepoint: Nil