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Comparative Evaluation of Implant Stability, Soft & Hard Tissue Healing Around UV Activated vs Conventional Implants

K

Krishnadevaraya College of Dental Sciences & Hospital

Status

Enrolling

Conditions

UV Dental Implant

Treatments

Procedure: UV implant
Procedure: conventional implant

Study type

Interventional

Funder types

Other

Identifiers

NCT06541912
02_D012_00048

Details and patient eligibility

About

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

Full 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.

Enrollment

12 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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
  • Smokers
  • Patients who are psychologically unable to participate
  • Poor oral hygiene

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Single Blind

12 participants in 2 patient groups

conventional dental implant group
Active Comparator group
Description:
conventional dental implant placement will act as control group.
Treatment:
Procedure: conventional implant
UV dental implant group
Experimental group
Description:
UV activated implant placement will act as test group which has better osseointegration properties.
Treatment:
Procedure: UV implant

Trial contacts and locations

1

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Central trial contact

Dr. PRABHUJI MLV, MDS; Dr. shailja dutta, mds

Data sourced from clinicaltrials.gov

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