New study tests High-Tech bladder diary for better diagnosis
NCT ID NCT05702294
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether an automated measuring device can improve the accuracy of bladder diaries in women with lower urinary tract symptoms. 187 women recorded their urine volume using both a traditional paper diary and an electronic device. The goal was to see if the device provides more precise data to help doctors diagnose and treat bladder problems.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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187 people
The number who actually took part.
- Started
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Sep 2022
- Finished
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Aug 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Eligibility criteria for females with lower urinary tract symptoms: Inclusion Criteria: * Females * 18 years of age or above * Females presenting with lower urinary tract symptoms Exclusion Criteria: * Females who have a mental/physical disability which would make them unable to understand/comply with the requirements of the study. Eligibility criteria for healthy volunteers: Inclusion criteria * Female * 18 years of age or above Exclusion criteria * Females who have a mental/physical disability which would make them unable to understand/comply with the requirements of the study. * Female with (LUTS).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Birmingham Women's and Children's Hospital
Birmingham, B15 2TG, United Kingdom
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