- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01749527
Does Patient Activity Level Affect 24-Hour Pad Test Results in Stress-Incontinent Women
December 12, 2012 updated by: Emmanuel Karantanis, St George Hospital, Australia
Does Patient Activity Level Affect 24-Hour Pad Test Results in Stress-Incontinent Women?
We hypothesised that in women with stress urinary incontinence, the severity of leakage on a 24 hour pad test was affected by activity.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
We asked women to perform two separate pad tests, one with normal activity, and another with decreased activity.
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Stress urinary incontinence
Exclusion Criteria:
- language other than english
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: 24-hour pad test
decreased activity
|
Pad test with minimal activity
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
24-hour pad test weight gain (mls)
Time Frame: 24 hours
|
24 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2006
Primary Completion (Actual)
December 1, 2006
Study Completion (Actual)
December 1, 2006
Study Registration Dates
First Submitted
December 11, 2012
First Submitted That Met QC Criteria
December 12, 2012
First Posted (Estimate)
December 13, 2012
Study Record Updates
Last Update Posted (Estimate)
December 13, 2012
Last Update Submitted That Met QC Criteria
December 12, 2012
Last Verified
December 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Activity Study
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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