Improving Bone Density with Osseodensification After Delayed dental implant placement: A clinical study after delayed implant placement: A clinical and radiographic study

Phase 2/3

Not yet recruiting

• Conditions: Atrophy of edentulous alveolar ridge,

• Registration Number: CTRI/2025/03/082513
• Lead Sponsor: Datta Meghe Institute of Higher Education and Research

Brief Summary

This research study aims at assessing the efficiency of theOsseodensification (OD) system in enhancing the bone density and volume incases with delayed implant placement. It assesses the OD impact on the healingof bones and osseointegration, which is by comparing the clinical andradiographic outcomes before surgery and after it.This is a six-month single-armclinical and radiographic study in 10 systemically healthy patients withedentulous regions in the anterior or posterior arch. Pre-operative full-mouthultrasonic scaling, dental hygiene instructions, and pre-operative CBCT imagingwill be obtained to measure the bone density at the apical, mesial, and distalregions of the extraction socket in Hounsfield units. Following localanesthesia and implant surgery, osseodensification will be applied to increasethe density of the bone at the time of preparation of the implant site.Postoperative care will include antibiotics, anti-inflammatory drugs, andfollow-up visits. Cone Beam Computed Tomography (CBCT) imaging will be done atbaseline, 3 months, and 6 months post-surgery to monitor changes in bonedensity. Implant mobility will be measured using the Clinical Implant MobilityScale (CIMS).

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2025-03-13
• Study Start: 2025-04-15

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

• 1.Thick gingival biotype.
• 2.Radiographic and clinical appearance of intact alveolar bony walls.
• 3.4 mm of bone radiographically at root apex 4.D-2 or D-3 bone quality.

Exclusion Criteria

• 1.Uncontrolled systemic conditions (e.g., diabetes, cardiovascular diseases).
• 2.Severe periodontal disease or active infections.
• 3.Insufficient bone requiring advanced grafting.
• 4.Pregnant or breastfeeding women.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
primary stability include enhanced mechanical retention of the implant due to increased bone density around the implant site.	CBCT will be taken pre operatively, 3months and after 6 months of implant placement and bone density in Hounsfield unit will be checked.

Trial Locations

Locations (1)

Sharad Pawar Dental College; 🇮🇳 Wardha, MAHARASHTRA, India

Sharad Pawar Dental College

🇮🇳Wardha, MAHARASHTRA, India

Dr Rutuja Karamore

Principal investigator

09422282446

rutujakaramore125@gmail.com