A study to compare bone density and implant stability using two different implant drilling methods in the posterior region of the jaw

Phase 2

• Conditions: Health Condition 1: K084- Partial loss of teeth

• Registration Number: CTRI/2023/01/049279
• Lead Sponsor: A R Sanofar

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 February 2023

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Adequate bone height and width after extraction to accommodate the implant without impinging on vital structures in either maxillary or

mandibular arches.

2. Bone density range between <=850 and >=150 measured in Hounsefield units based on CBCT findings (corresponding to D3 -D4 bone density according to bone density classification by Misch).

3. Medically fit participants of age range between 24 â?? 50 years.

4. Willingness to participate for the duration of the study.

5. General good health

6. Patient who will give positive informed consent.

7. Both the edentulous areas having antagonist teeth.

Exclusion Criteria

1. High bone density (more than 850 HU corresponding to D1and D2 level of bone density classification by Misch),

2. Bone metabolic disorders such as osteoporosis, osteomalacia, rickets affecting surrounding bone health.

3. History of radiotherapy in head and neck region.

4. Current habit of smoking or alcohol or drug abuse.

5. Systemic conditions as uncontrolled diabetic and hypertensive patients and cardiovascular conditions affecting the integrity of implant or

connective tissue health surrounding the implant.

6. Bleeding dyscrasias or under anticoagulant therapy.

7. Needed augmentation of the implant site.

8. Signs of infection in the prospective implant site.

9. History of participants undertaking

systemic corticosteroids, bisphosphonates or any other medications that would compromise postoperative healing or osseointegration.

10. Pregnancy / lactating mothers at the

time of enrollment.

11. Parafunctional habits such as bruxism and clenching,

12. Local limitations such as inadequate inter-ridge distance

13. Poor oral hygiene and motivation

14. Untreated generalized periodontitis.

15. Full mouth plaque and the bleeding

score of 15 % or less.

Study & Design

• Study Type: Interventional
• Study Design: Not specified