Validity and Reliability of ICIQ-FLUTS LF in Thai Version and Correlation With IPSS
NCT ID: NCT06270849
Last Updated: 2024-02-21
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
130 participants
OBSERVATIONAL
2023-02-24
2024-01-20
Brief Summary
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Detailed Description
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The normal control group 80 women will completed ICIQ-FLUTS LF for test of construct validity.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Female with LUTS
Females who has symptoms of lower urinary tract symptoms
Questionnaire
The questionnaire to assess severity of LUTS in women.
Normal control group
Females who no history of LUTS or urinary tract disease
Questionnaire
The questionnaire to assess severity of LUTS in women.
Interventions
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Questionnaire
The questionnaire to assess severity of LUTS in women.
Eligibility Criteria
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Inclusion Criteria
* can read and understand Thai language
* have lower urinary tract symptoms
Exclusion Criteria
18 Years
60 Years
FEMALE
Yes
Sponsors
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Thammasat University Hospital
OTHER
Responsible Party
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Valeerat Swatesutipun
Principle investigator
Principal Investigators
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Valeerat Swatesutipun, MD
Role: PRINCIPAL_INVESTIGATOR
Thammasat University Hospital
Locations
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Thammasat University Hospital
Khlong Luang, Changwat Pathum Thani, Thailand
Countries
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Other Identifiers
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MTU-EC-SU-0-002/66
Identifier Type: -
Identifier Source: org_study_id
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