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Clinical Trials/NCT06541912
NCT06541912
Recruiting
Not Applicable

Comparative Evaluation of Implant Stability, Soft and Hard Tissue Healing Around UV Activated Versus Conventional Implants - A Randomized Clinical Trial.

Krishnadevaraya College of Dental Sciences & Hospital1 site in 1 country12 target enrollmentFebruary 15, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
UV Dental Implant
Sponsor
Krishnadevaraya College of Dental Sciences & Hospital
Enrollment
12
Locations
1
Primary Endpoint
Implant stability using Resonance Frequency Analysis
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

Research is to compare and evaluate the primary and secondary implant stability, healing of the soft tissue around UV activated implants and conventional implants.

Detailed Description

Research is to compare and evaluate the primary and secondary implant stability, healing of the soft tissue around UV activated implants and conventional implants. The objectives are to access the primary and secondary implant stability using Resonance frequency analysis, marginal bone level using RVG with grid, healing of the soft tissue. The control group will be treated with conventional implant and test group will be treated with UV implants. The total number of participants are 12 and 24 sites (control - 12 sites, test - 12 sites) with 3 months follow up.

Registry
clinicaltrials.gov
Start Date
February 15, 2024
End Date
March 25, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Krishnadevaraya College of Dental Sciences & Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • At east above 18 years of age
  • Patients who needs replacement for at least 2 missing teeth in the posterior region of mandible
  • Adequate bone volume to accommodate planned dental implants
  • Patients who will comply with oral health care instructions and necessary visits

Exclusion Criteria

  • General contraindications to dental implant treatment ( uncontrolled diabetes, severe cardiovascular or infectious disease)
  • Intravenous and oral bisphosphonate therapy
  • Unwillingness to return for the follow up examinations
  • Patients who are psychologically unable to participate
  • Poor oral hygiene

Outcomes

Primary Outcomes

Implant stability using Resonance Frequency Analysis

Time Frame: "Immediately after Post-operative", "1 month", "3 months"

to measure primary and secondary stability

Secondary Outcomes

  • Marginal bone loss using RVG with grid("Immediately after Post-operative", 3 months)
  • Soft tissue healing(1 week, 1 month, 3 months.)

Study Sites (1)

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