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The effect of bone graft use with low-level laser therapy in the treatment of periodontal disease

A comparative study of autogenous bone graft use with and without low-level laser therapy in the treatment of the two and three wall intrabony periodontal defects

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201207019121N2
Enrollment
15
Registered
2012-07-22
Start date
2011-05-01
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

Chronic periodontitis. Chronic pericoronitis

Interventions

Intervention 1: Control group: Regenerative surgery under local anesthesia of Lidocaine 2% with epinephrine 1/80000- sulcular incision in baccal and lingual aspects and debridement of the lesion with
Treatment - Surgery
Control group: Regenerative surgery under local anesthesia of Lidocaine 2% with epinephrine 1/80000- sulcular incision in baccal and lingual aspects and debridement of the lesion with hand instruments
Intervention in test group: Regenerative surgery under local anesthesia of Lidocaine 2% with epinephrine 1/80000- sulcular incision in baccal and lingual aspects and debridement of the lesion with han

Sponsors

Tabriz university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Full mouth plaque index (FMPI) <= 20%; the percentage of the areas which are bleeding within 30 seconds after the probe be less than or equal to 20%; in the radiographic assessment which was confirmed with bone sounding, each patient has at least one pair similar infra-bony defects in the interproximal region with probing depth greater or equal to 5 mm and lesion depth of equal to or greater than 3 mm. Exclusion criteria: presence of systemic disease interfering with periodontal surgery or healig; smoking; trauma from occlusion; prolonged use of drugs interfering with bone metabolism; pregnancy and lactation; antibiotic use during study or in the past 6 months.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bone fill of the intrabony defect. Timepoint: baseline, three months later. Method of measurement: UNC-15 probe.

Secondary

MeasureTime frame
Clinical attachment level. Timepoint: baseline, 3 months. Method of measurement: UNC 15.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mehrnoosh Sadighi

Tabriz dental faculty

mehrnoosh1378@yahoo.com+98 41 1335 5965

Outcome results

None listed

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