A clinical trial to assess the effect of change in bone levels following implant placement immediately after removal of tooth with and without socket shield (leaving a tooth root section)
Phase 3
- Conditions
- Health Condition 1: null- Healthy
- Registration Number
- CTRI/2018/06/014610
- Lead Sponsor
- Divya Das
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Systemically healthy adults who present with hopeless teeth indicated for extraction and are willing for immediate implant placement.
Tooth indicated for extraction should be periodontally healthy.
Non smoker
Exclusion Criteria
Systemically unhealthy
Teeth with present / past periodontal disease
Teeth with vertical root fractures on the buccal aspect
Teeth with horizontal fractures at / below bone level
Teeth with external / internal resorption of buccal part of root
Patients who are pregnant, intending to conceive or breast feeding
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the dimensional alterations in bone level (buccal plate) radiographically (CBCT) and clinically by transgingival probing at baseline, 3 months and at 6 months.Timepoint: Baseline, 3 months and at 6 months
- Secondary Outcome Measures
Name Time Method To evaluate the soft tissue around the implant using the Pink Esthetic Score (PES), implant mobility and signs of peri â?? implantitis. Assessment of pain threshold and patient satisfaction using Visual Analogue Scale (VAS).Timepoint: The soft tissue around the implant will be assessed using the Pink Esthetic Score (PES). Assessment of implant mobility and signs of peri â?? implantitis will be evaluated. Assessment of pain threshold and patient satisfaction using Visual Analogue Scale (VAS)at baseline, 3 months and at 6 months.