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The effect of Low level laser in biomaterial used in maxillary sinus graft

The effect of Low level laser in biomaterial used in maxillary sinus graft (histological and Radiological examination) a randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016012410155N3
Enrollment
19
Registered
2016-02-22
Start date
2016-01-30
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Resorption of alveolar ridge in the maxillary posterior region. Atrophy of edentulous alveolar ridge

Interventions

Intervention 1: The sinus floor of control group will be augmented with lateral window sinus lift surgical technique by using biomaterials (allograft + PFR). Intervention 2: Intervention group:Surgica
Treatment - Surgery
The sinus floor of control group will be augmented with lateral window sinus lift surgical technique by using biomaterials (allograft + PFR)
Intervention group:Surgical technique and biomaterials is similar to the control group, with the difference that immediately after the surgery and the third and fifth days after surgery, low level las

Sponsors

Gingival and Dental Research Center of Tabriz dentistry Faculty
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:The existence of bilaterally partial edentulous in maxillary posterior region or complete edentulous in maxilla; Height of the remaining bone between the floor of sinus and alveolar crest be less than 5mm Exclusion criteria:Smokers; pregnant women ; pathological symptoms or cystic lesions in the sinus ; acute and chronic inflammatory disease of sinus; benign and malignant tumors in sinus ;uncontrolled systemic diseases ; the existence of untreated periodontal disease

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The newly formed bone. Timepoint: 5 months after grafting. Method of measurement: Histologic examination and measurements through the via software motic images plus v2.0.;Evaluation of The newly formed bone density. Timepoint: 5 months after grafting. Method of measurement: By CBCT and NNT viewer Version21 software.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Alihossein Dehghani

Faculty of Dentistry

a_h_dehgani@yahoo.com+98 41 3335 5968

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026