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Evaluation of photo biomodulation using low level laser therapy in terms of stability of dental implant

Phase 3
Conditions
Health Condition 1: K084- Partial loss of teeth
Registration Number
CTRI/2023/10/058685
Lead Sponsor
Saveetha Dental
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

with bilateral edentulousness in opposing quadrants. Emphasis was placed on individuals with good health, devoid of any systemic conditions or periodontally compromised dentition. Another crucial factor was the presence of sufficient amounts of available alveolar bone, sufficient to accommodate the standard dental implant size (3.5 by 11.5 millimeters) for both implant sites

Exclusion Criteria

Patients with a history of systemic diseases or conditions, such as uncontrolled diabetes or immunodeficiency disorders, which could potentially compromise the success of dental implant surgery and osseointegration, were excluded. Furthermore, those who were smokers or users of tobacco products were not considered, given their propensity to hinder positive outcomes. Individuals with a prior history of radiation therapy to the head and neck region, pregnant or lactating mothers, and those who had previously received dental implants in the same region were also excluded.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
implant stability quotient using a radio frequency analysis deviceTimepoint: baseline (immediately after implant placement), 1 week, 2 week, 4 weeks, 12 weeks post surgery, during follow ups
Secondary Outcome Measures
NameTimeMethod
patient overall satisfaction, quality of life.Timepoint: restorative phase (6 months post implant placement - end of trial)
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