loss of teeth.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The applicants of implant treatment that two-sided in a jaw in a similar area have lost tooth. tooth extraction at least 6 months before implant surgery; nongrafted implant site; type 2 or 3 bone quality according to the Lekholm and Zarb classification, adequate space with buccolingual width of minimum 6 mm and mesiodistal width of minimum 7 mm; inter-occlusal distance greater than 7 mm.
Exclusion criteria
Exclusion criteria: Pregnant women. Any mental illness and psychological and behavioral conditions, which is the absolute contraction of implant treatment. Any systemic illness that contraindicates surgery; uncontrolled diabetes mellitus; bisphosphonate therapy; history of radiotherapy in the maxillofacial region within last 12 months; smoking; para-functional habits; poor oral hygiene with full mouth plaque score and full mouth bleeding score =25%, periodontally compromised patients with attachment loss =3 mm, and/or radiographic bone loss =30% of root length in =30% of sites and those who refused to return for follow-up were excluded from this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measuring crestal bone levels around dental implants by radiography. Timepoint: Crestal bone level at 4 time 1) immediately after receiving of 940 nm (T0) laser (T0) 2) 6 weeks after receiving laser diode 940 nm (T1) 3) 6 months after receiving low-laser diode 940 nm (T2) Using parallel-based digital periametic radiography, measured by parallel technique. Method of measurement: Using parallel-based digital periametic radiography, measured by parallel technique. | — |
Countries
Iran (Islamic Republic of)
Contacts
Arak University of Medical Sciences