Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
50 participants
INTERVENTIONAL
2021-04-25
2022-04-25
Brief Summary
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Materials and Methods: According to the study protocol, patients, who were diagnosed with peri-implantitis based on the clinical and radiographic evaluations, were divided into six groups: Group 1: smokers undergoing diode laser application; Group 2: smokers undergoing Erbium, chromium: yttrium, scandium, gallium, garnet (Er, Cr:YSGG) laser application; Group 3: smokers undergoing Erbium:yttrium-aluminum-garnet (Er:YAG) laser application; Group 4: non-smokers undergoing diode laser application; Group 5: non-smokers undergoing Er, Cr:YSGG laser application; and Group 6: non-smokers undergoing Er:YAG laser application. Peri-implant sulcus depth (SD), clinical attachment level (CAL), suppuration, modified plaque index (mPI), gingival index (GI), and modified sulcus bleeding index (mSBI) were recorded and peri-implant sulcus fluid (PISF) was collected to evaluate osteocalcin.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Diode laser
Lasers
The laser tip was applied as vertical and horizontal scan along the subgingival implant . The procedure was carried out on day zero, seven and 14.
Er,Cr:YSGG laser
Lasers
The laser tip was applied as vertical and horizontal scan along the subgingival implant . The procedure was carried out on day zero, seven and 14.
Er:YAG LAser
Lasers
The laser tip was applied as vertical and horizontal scan along the subgingival implant . The procedure was carried out on day zero, seven and 14.
Interventions
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Lasers
The laser tip was applied as vertical and horizontal scan along the subgingival implant . The procedure was carried out on day zero, seven and 14.
Eligibility Criteria
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Inclusion Criteria
2. No mobility in implant
3. Implants with bridge foot and opposite occlusion
4. Having no systemic disease that may affect the outcome of treatment
5. No systemic use of antibiotics for the last six months
6. Not receiving peri-implantitis treatment for the last three months
7. Individuals at the 30-60 years of age.
Exclusion Criteria
2. Individuals receiving radiation therapy
3. Individuals using alcohol
4. Presence of pregnancy and lactation period
5. Individuals with parafunctional habits such as clenching or bruxism.
30 Years
60 Years
ALL
No
Sponsors
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Kırıkkale University
OTHER
Responsible Party
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Kubilay BARIŞ
dr.
Locations
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Kırıkkale University faculty of Dentistry
Yahşihan, Kırıkkale, Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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Interventional
Identifier Type: -
Identifier Source: org_study_id
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