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
3000 participants
OBSERVATIONAL
2014-06-30
2015-11-30
Brief Summary
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The population is contacted and asked for informed consent, whereafter a questionnaire of about 200 questions, used in a number of studies in clinical studies and trials, are sent out.
The results will be used as reference values to our patient cohorts
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* no informed consent
30 Years
89 Years
ALL
No
Sponsors
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Sahlgrenska University Hospital
OTHER
Eva Haglind
OTHER
Responsible Party
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Eva Haglind
Professor, Consultant Surgeon
Principal Investigators
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Eva Haglind
Role: PRINCIPAL_INVESTIGATOR
Department of Surgery, Institure for Clinical Sciences, Sahlgernska Academy at Göteborg University
Locations
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Göteborg University, Sahlgrenska Academy, Inst Clinical Sciences, Dept Surgery,
Gothenburg, , Sweden
Countries
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References
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Bock D, Angenete E, Gonzales E, Heath J, Haglind E. Assessing health, quality of life and urogenital function in a sample of the Swedish general population: a cross-sectional study. BMJ Open. 2018 May 5;8(5):e021974. doi: 10.1136/bmjopen-2018-021974.
Other Identifiers
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QoL normal Swedes
Identifier Type: -
Identifier Source: org_study_id
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