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
30 participants
INTERVENTIONAL
2019-01-01
2021-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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PRF application
Patients with alveolar osteitis in which PRF application was performed.
PRF application
PRF application into post-operative wound.
Aspirin application
Patients with alveolar osteitis in which Nipas was used.
Nipas application
Nipas application into post-operative wound.
Interventions
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PRF application
PRF application into post-operative wound.
Nipas application
Nipas application into post-operative wound.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* patients with symmetric teeth qualified for extraction,
Exclusion Criteria
* patients allergic to acetylsalicylic acid ,
* systemic diseases,
* pregnancy,
* lactation,
* drugs known to affect the number or function of platelets,
* abnormal platelet counts,
18 Years
70 Years
ALL
Yes
Sponsors
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Medical University of Lodz
OTHER
Responsible Party
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Principal Investigators
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Anna Janas-Naze, Prof.
Role: PRINCIPAL_INVESTIGATOR
Medical University of Lodz
Locations
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Department of Oral Surgery
Lodz, , Poland
Countries
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Other Identifiers
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0002
Identifier Type: -
Identifier Source: org_study_id
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