An experimental study for checking the superiority of the metal framework design of porcelain-fused-to-metal prosthesis made by using a newly designed device and conventional design.
Phase 4
- Registration Number
- CTRI/2024/03/063646
- Lead Sponsor
- Dr Prabha Shakya Newaskar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients with missing mandibular missing mandibular second premolar, mandibular first molar, mandibular first & second premolar and mandibular second premolar & first molar teeth.
2. Patient who is ready to give consent.
3. Patient with healthy periodontium.
4. Patient with Permanent dentition (no retained deciduous teeth).
Exclusion Criteria
1.Patient with absolute contraindication for fixed partial denture.
2.Patient who is not willing for fixed partial denture.
3.Mentally challenged pt.
4.Patient with any gingival and periodontal pathology.
5.Patient with compromised abutment periodontal health.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bleeding on probing, Veneer chipping & Marginal ditchingTimepoint: 0, 3, 6 months
- Secondary Outcome Measures
Name Time Method To evaluate superiority and clinical utility of newly design framework as compared to conventional framework.Timepoint: 0,3,6 Months