Skip to content

Low Level Laser Therapy in Postsurgical Treatment of Grafted Sockets

Histological Evaluation of the Efficiency of Low Level Laser Therapy on Bone Regeneration in Grafted Tooth Sockets

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615001013550
Enrollment
46
Registered
2015-09-29
Start date
2014-07-21
Completion date
2015-01-14
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The aim of this study is to determine whether low level laser therapy can decrease the time between extraction/socket graft and implant placement, by evaluating histological changes in sockets grafted with bone graft material and covered with resorbable collagen dressing

Interventions

Autostatic laser device which patient self-administers at home, pointing at site of grafted socket, starting in day 14 after surgery Low level laser therapy on the site of grafted sockets; 810nm, 20mW/square cm, 20 min per day, 21 consecutive days Laser device composed of a comfortable flexible headset, lightweight, low profile, with a soft nose and earpice for individual comfort profile and array positioning to fit range of patients; and a handsfree operation controller. On this controller the

Autostatic laser device which patient self-administers at home, pointing at site of grafted socket, starting in day 14 after surgery Low level laser therapy on the site of grafted sockets; 810nm, 20mW/square cm, 20 min per day, 21 consecutive days Laser device composed of a comfortable flexible headset, lightweight, low profile, with a soft nose and earpice for individual comfort profile and array positioning to fit range of patients; and a handsfree operation controller. On this controller the doctor sets treatment protocol and the controller counts down time and treatment sessions for patients awareness

Sponsors

Adriana Monea
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

systemically healthy subjects, no chronic treatment for any systemic disease, no active infection present at the time of extraction, 5 wall-extraction/ wall defects, undergoing tooth extract surgery in which sockets grafted with bone graft material and covered with resorbable collagen dressing

Exclusion criteria

periapical lesions immediate post-surgical complications such as loose membrane or loose bone graft material

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026