Alterations in Connective Tissue in Patients With or Without Pelvic Organ Prolapse
NCT ID: NCT01749696
Last Updated: 2014-05-09
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
78 participants
OBSERVATIONAL
2009-11-30
2014-04-30
Brief Summary
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Detailed Description
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The formalin-fixed and paraffin embedded tissue samples were stained with Verhoeff van Gieson and Movat's pentachrome. Samples were examined by pathologist and gynecologist blinded as to the other investigator and to the pelvic organ prolapse status. In case of discrepancy investigators evaluated the samples together to gain consensus.
Conditions
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Study Groups
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Patients with pelvic organ prolapse
Patients, who were operated on because of pelvic organ prolapse.
No interventions assigned to this group
Patients without pelvic organ prolapse
Patients, who had hysterectomy due to other reasons than pelvic organ prolapse.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* hysterectomy due to other benign reasons than pelvic organ prolapse
Exclusion Criteria
FEMALE
No
Sponsors
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Turku University Hospital
OTHER_GOV
Responsible Party
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Locations
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Department of Obstetrics and Gynecology, Turku University Central Hospital
Turku, , Finland
Countries
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Other Identifiers
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33/180/2009
Identifier Type: -
Identifier Source: org_study_id
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