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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COMPLETED
48 participants
OBSERVATIONAL
2018-08-15
2020-03-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Endometrioma
Endometrioma (n=23)
Adropin (ng/L)
Thawed samples were measured on a Molecular Devices SpectraMax i3 Multi-Mode, Microplate Reader (batch number: SER 35 370-1448, made in Austria) using enzyme linked immunosorbent assay (ELISA).
Healthy controls
Healthy controls Healthy volunteers n=25
Adropin (ng/L)
Thawed samples were measured on a Molecular Devices SpectraMax i3 Multi-Mode, Microplate Reader (batch number: SER 35 370-1448, made in Austria) using enzyme linked immunosorbent assay (ELISA).
Interventions
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Adropin (ng/L)
Thawed samples were measured on a Molecular Devices SpectraMax i3 Multi-Mode, Microplate Reader (batch number: SER 35 370-1448, made in Austria) using enzyme linked immunosorbent assay (ELISA).
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* chronic kidney disease (CKD),
* CAD,
* heart failure (HF),
* cerebrovascular accident (CVA),
* malignancy,
* rheumatoid disorder,
* liver disease, and
* active infections were excluded from the study.
18 Years
FEMALE
Yes
Sponsors
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Muğla Sıtkı Koçman University
OTHER
Responsible Party
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Burak Sezgin
Principal Investigator
Principal Investigators
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Burak Sezgin, Dr
Role: PRINCIPAL_INVESTIGATOR
Mugla Sıtkı Kocman University Faculty of Medicine
Locations
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Mugla Sıtkı Kocman University Faculty of Medicine
Muğla, , Turkey (Türkiye)
Countries
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Other Identifiers
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22/08/2019-05
Identifier Type: -
Identifier Source: org_study_id
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