To check the bone changes after immediate dental implant placement

Phase 2

Conditions: Health Condition 1: null- 15 patients who need extraction for trauma, endodontic treatment failure, or non-restorable carious teeth, teeth.

Registration Number: CTRI/2017/10/009979

Lead Sponsor: Sinhgad Dental College and Hospital

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Open to Recruitment

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

1.Systemically healthy patients between the age group of 20-65 years with teeth indicated for extraction and future prosthesis.

2.Good oral hygiene defined as a full mouth plaque score <25%(Oâ??Leary et al, 1972)

3.Indications for extraction include trauma, endodontic treatment failure, or non-restorable carious teeth, teeth with healthy periodontium, alveolar sockets with 4 wall architecture and intact labial plate.

4.Ideal soft tissue level and contour at the facial aspect of the failing tooth and thick gingival biotype as determined by De Rouck et al(2009)

5.Teeth should have adequate residual apical bone below the tooth >= 4 mm.

6.Patients willing to participate and sign an informed consent.

7.Patients who are compliant.

Exclusion Criteria

1.Systemic conditions contraindicating surgical intervention

2.Immediately placed implants that have failed before the prosthetic loading.

3.Patients having history of severe bruxism and/or clenching habits.

4.Smokers.

5.Patient having history of bone disorder.

6.Teeth having acute periapical or periodontal pathology before the extraction.

7.Pregnant and lactating females.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Horizontal measurement: <br/ ><br>1. distance from the external surface of the buccal and Palatal/lingual alveolar plates to the implant surfaces <br/ ><br>2.distance from external surface of the buccal alveolar plate to the external surface of the palatal/lingual alveolar plate (buccolingual width) <br/ ><br> <br/ ><br>Vertical facial bone level will be measured on facial surface of the implant as the perpendicular distance from the implant platform to the most coronal point of the facial bone. <br/ ><br>Timepoint: The sites will be evaluated radiographically at baseline (day of immediate loading) and 6 months after loading.

Secondary Outcome Measures