Quality of Life After Conservative and Surgical Treatment of Pelvic Organ Prolapse
NCT ID: NCT04110821
Last Updated: 2024-07-30
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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RECRUITING
134 participants
OBSERVATIONAL
2019-09-15
2028-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients unable to understand an informed consent
* Patients unwilling to participate
* emergency operations
* pregnancy
* Overactive Bladder without descensus
* Stool incontinence without POP
18 Years
ALL
No
Sponsors
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University Hospital, Basel, Switzerland
OTHER
Responsible Party
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Principal Investigators
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Daniel Steinemann, PD Dr. med.
Role: PRINCIPAL_INVESTIGATOR
University Hospital Basel, Clarunis
Locations
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University Hospital Basel/Dep. of Visceral Surgery (Clarunis)
Basel, , Switzerland
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2019-01190
Identifier Type: -
Identifier Source: org_study_id
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