Influence of bone quantity in determining Implant success in upper front teeth region

Phase 1

Not yet recruiting

• Conditions: Encounter for fitting and adjustment of dental prosthetic device,

• Registration Number: CTRI/2020/09/027694
• Lead Sponsor: RAJIV GANDHI UNIVERSITY OF HEALTH SCIENCES

Brief Summary

The study is designed witha aim of evaluating the thickness of the palatal bone and buccolingualangulation of the maxillary anterior teeth in 3 dimensional positioning of theimmediate implant placement and provisionalization. With these objectives,

Ø To determine the correlation between the angulation of thetooth and angulation of the implant in achieving primary stability

Ø To evaluating the response of the labial cortical plate at 12months interval.

Ø To measure the torque value, primary stability and secondaryimplant stability.

Ø To evaluate the horizontal and vertical dimensional changesin the facial bone following immediate implant placement and provisionalizationin maxillary anterior region.

Ø To evaluate the aesthetic outcome.

The subject selection will be done according tothe inclusion and exclusion criteria, 30 subjects will be selected, pre-operativeassessment tooth indicated for IIPP and Virtual implant position and prosthesisis planned and this is executed with guided surgery. Immediate provisionalrestoration will be given and after 4 months definitive prosthesis will bedelivered. According to the number of recalls, dates per subject and studyduration will be day 1, after 1 week,  4months and after 12 months. This proposed study will allow surgeon toaccurately position the implant of ideal size in maxillary anterior regionengaging the palatal bone thereby reducing the surgical time, increases thebone implant contact, maintains the soft tissue contour and provides theprosthetic replacement in esthetically demand zone.

Detailed Description

Not available

Study Timeline

• Study Start: 2020-01-10
• Last Update Posted: 2020-02-09

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• 1.Patient with age group of 20-45 years with no significant medical history.
• 2.Tooth fractured secondary to trauma with intact alveolar bone 3.Grossly decayed tooth with no active infection 4.Endodontic failures with no acute infection and periapical pathology.
• 5.Presence of residual root/root fracture with intact labial bone.
• 6.Non restorable tooth.

Exclusion Criteria

• 1.Patients with uncontrolled periodontal disease, smokers, current alcohol or drug abuse, systemic conditions and medication that would interfere with wound healing or osseointegration, history of radiotherapy in the head and neck region, History of Chemotherapy, long term steroids.
• 2.Presence of active infections, dentoalveolar fracture.
• 3.Inadequate width/height of available bone 4.Patients with parafunctional habits.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ISQ 50 TORQUE 20Ncm PALATAL BONE AND LABIAL BONE THICKNESS	DAY 1 AT 4 AND 12 MONTHS

Secondary Outcome Measures

Name	Time	Method
AESTHETIC OUTCOME	MORPHOLOGICAL ASSESSMENT OF LABIAL BONE

Trial Locations

Locations (1)

RAJARAJESWARI DENTAL COLLEGE AND HOSPITAL; 🇮🇳 Bangalore, KARNATAKA, India

RAJARAJESWARI DENTAL COLLEGE AND HOSPITAL

🇮🇳Bangalore, KARNATAKA, India

DR MAMATHA N S

Principal investigator

9880194412

drmamathans@gmail.com