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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01749527
Other study ID # Activity Study
Secondary ID
Status Completed
Phase N/A
First received December 11, 2012
Last updated December 12, 2012
Start date March 2006
Est. completion date December 2006

Study information

Verified date December 2012
Source St George Hospital, Australia
Contact n/a
Is FDA regulated No
Health authority Australia: Department of Health and Ageing Therapeutic Goods Administration
Study type Interventional

Clinical Trial Summary

We hypothesised that in women with stress urinary incontinence, the severity of leakage on a 24 hour pad test was affected by activity.


Description:

We asked women to perform two separate pad tests, one with normal activity, and another with decreased activity.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date December 2006
Est. primary completion date December 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Stress urinary incontinence

Exclusion Criteria:

- language other than english

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms

  • 24-hour Pad Test Weight Gain With and Without Activity
  • Weight Gain

Intervention

Behavioral:
minimal activity
Pad test with minimal activity

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
St George Hospital, Australia

Outcome

Type Measure Description Time frame Safety issue
Primary 24-hour pad test weight gain (mls) 24 hours No