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NCT00754260 · ClinicalTrials.gov registry record · NA
Caffeine Reduction and Overactive Bladder Symptoms
A NA study, sponsored by University of New Mexico.
- Terminated
- Registry status
- NA
- Development phase
- 42
- Enrollment target
NCT00754260: Clinical Trial NA study, sponsored by University of New Mexico.
NCT00754260 is a NA study that was terminated before completion, run by University of New Mexico. The registered enrollment target is 42 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00754260, a NA study, was terminated before completion, sponsored by University of New Mexico.
- TERMINATED
- Registry status
- NA
- Development phase
- 42 participants
- Enrollment target
Study Summary
A. Statement of Objective: To conduct a randomized trial to evaluate the impact of caffeine restriction on Overactive Bladder(OAB) symptoms including urinary frequency, nocturia, incontinence episodes, symptom severity and bother and quality of life. B. Specific Aims/Hypothesis: 1. To determine if reduction in caffeine intake decreases urinary frequency, nocturia and incontinence episodes as measured on a 3-day voiding diary in women with Overactive Bladder (OAB). We hypothesize that women with overactive bladder will report less frequent urination and decreased nocturia and incontinence episodes with caffeine reduction. 2. To determine whether caffeine reduction results in decreased symptom severity and bother and improved quality of life scores as measured by the Questionnaire for Incontinence Severity Index (ISI), Questionnaire for Urinary Incontinence Diagnosis (QUID), Urogenital Distress Inventory (UDI-6) and the Incontinence Impact Questionnaire (IIQ-7). We hypothesize that women with OAB who reduce their intake of caffeine will report decreased symptom bother and improved quality of life as measured by the ISI, UDI-6 and the IIQ-
Interventions
- BEHAVIORAL Caffeine reduction
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 42 participants |
| Start Date | 2008-03 |
| Est. Completion | 2009-06-30 |
| Phase | NA |
Why NCT00754260 stopped before completion
NCT00754260 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 1 intervention - of which Caffeine reduction is the first listed.
NCT00754260 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00754260 about?
NCT00754260 is a clinical study titled "Caffeine Reduction and Overactive Bladder Symptoms". A. Statement of Objective: To conduct a randomized trial to evaluate the impact of caffeine restriction on Overactive Bladder(OAB) symptoms including urinary frequency, nocturia, incontinence episodes, symptom severity and bother and quality of life. B. Specific Aims/Hypothesis: 1. To determine if...
What is the current status of trial NCT00754260?
This trial is currently terminated. It is a NA study. The enrollment target is 42 participants. The study started on 2008-03. Estimated completion is 2009-06-30.
What interventions are being tested in trial NCT00754260?
The interventions under investigation include: Caffeine reduction (BEHAVIORAL).
Who is sponsoring clinical trial NCT00754260?
This trial is sponsored by University of New Mexico, which has 168 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00754260's enrollment target sits among peer trials
42 1436th of 2000 higher than 555 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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