MedPath

Can Combination of Low-Level Laser and Light-Emitting Diodes Enhance Stability of Dental Implants?

Not Applicable
Completed
Conditions
Dental Implant Healing
Interventions
Device: Low-Level Laser and Light-Emitting Diodes
Device: Dental implant placement
Registration Number
NCT03362307
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Subjects were assigned in two groups: In group 1, subjects received LLL and LED 20 min/day for 10 days after implant insertion, subjects in group 2did not undergo LLL and LED. implant stability quotients(ISQs) were measured in 0,10,21,42 and 63 days after implant placement.

Detailed Description

Subjects eligible for study inclusion had an edentulous area at the first molar of the mandible and needed a dental implant. Subjects were excluded from study enrollment if they had any diseases that affect bone, smoking, insufficient bone in the edentulous area which needs bone augmentation, failed to return for follow-up, or refused study enrollment.

All implants were placed at least 3 months after tooth removal. The size of implants was 4.8X 10 mm (Zimmer, USA) Subjects were aligned based on computer randomization in two groups: In group 1(intervention), subjects received LLL and LED after implant placement and in group 2 (control) the same device was used while device was off.

A portable device was applied for irradiation of the intervention group with combination of 810nm laser and 632nm LED.

Subjects in group 1 underwent LLL 15 mw/cm2 and LED 10 mw/cm2 20 min every day for 10 days.

The mesiodistal and buccolingual directions were measured and the mean implant stability quotients (ISQs) were determined. The RFA measurements were performed in immediate after insertion (time0) 10 days (time1), 3 weeks (time2), 6 weeks(time3) and 9(time 4) weeks after implant placement.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
28
Inclusion Criteria
  • subjects eligible for study inclusion had an edentulous area at the first molar of the mandible and needed a dental implant
Read More
Exclusion Criteria
  • . Subjects were excluded from study enrollment if they had any diseases that affect bone, smoking, insufficient bone in the edentulous area which needs bone augmentation, failed to return for follow-up, or refused study enrollment.
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Non Emitting groupDental implant placementIn laser emitiiing group, subjects received Low-Level Laser and Light-Emitting Diodes after implant placement and in Non-emitting group,the same device was used while device was off.
Laser Emitting groupLow-Level Laser and Light-Emitting Diodessubjects received Low-Level Laser and Light-Emitting Diodes after implant placement
Non Emitting groupLow-Level Laser and Light-Emitting DiodesIn laser emitiiing group, subjects received Low-Level Laser and Light-Emitting Diodes after implant placement and in Non-emitting group,the same device was used while device was off.
Laser Emitting groupDental implant placementsubjects received Low-Level Laser and Light-Emitting Diodes after implant placement
Primary Outcome Measures
NameTimeMethod
Resonance frequency analysisNine weeks after implant placement(time 4)

The stability of the implants was evaluated with resonance frequency analysis by the Osstell device

Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath