The Best Parameter of Bladder Diary Correlates With the Volume at Strong Desire to Void of Filling Cystometry

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
National Taiwan University Hospital
ClinicalTrials.gov Identifier:
NCT01776593
First received: January 18, 2013
Last updated: January 23, 2013
Last verified: January 2013
  Purpose

To identify the bladder diary parameters that are best correlated to VSD.


Condition
Bladder Diary
Urodynamic Studies

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective
Official Title: The Best Parameter of Bladder Diary Correlates With the Volume at Strong Desire to Void of Filling Cystometry

Resource links provided by NLM:


Further study details as provided by National Taiwan University Hospital:

Primary Outcome Measures:
  • To identify the bladder diary parameter that is best correlated to the volume at strong desire to void of filling cystometry. [ Time Frame: 1 week ] [ Designated as safety issue: No ]
    To identify which bladder diary parameter that is best correlated to the volume at strong desire to void of filling cystometry. Thus, that bladder diary parameter may be used as a surrogate for the volume of strong desire to void of filling cystometry and without the need of urodynamic studies.


Enrollment: 900
Study Start Date: April 2012
Study Completion Date: July 2012
Primary Completion Date: July 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts
Lower urinary tract symptoms

Detailed Description:

To identify the bladder diary parameters that are best correlated to VSD.

  Eligibility

Ages Eligible for Study:   20 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Female patients with lower urinary tract symptoms

Criteria

Inclusion Criteria:

  • Female patients with lower urinary tract symptoms who had underwent urodynamic studies

Exclusion Criteria:

  • Patients without data of bladder diary
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01776593

Locations
Taiwan
Department of Obstetrics & Gynecology, National Taiwan University Hospital
Taipei, Taiwan, 100
Sponsors and Collaborators
National Taiwan University Hospital
  More Information

No publications provided

Responsible Party: National Taiwan University Hospital, Professor, Ho-Hsiung Lin
ClinicalTrials.gov Identifier: NCT01776593     History of Changes
Other Study ID Numbers: 201203078RIC
Study First Received: January 18, 2013
Last Updated: January 23, 2013
Health Authority: Taiwan: Department of Health, Executive Yuan.

Keywords provided by National Taiwan University Hospital:
bladder capacity; bladder diary; bladder oversensitivity; lower urinary tract symptoms

ClinicalTrials.gov processed this record on October 22, 2014