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Brody Belt - Alternative Method of Securing a Patient's Urinary Drainage Bag

This study has been terminated.
(low accrual)
Sponsor:
ClinicalTrials.gov Identifier:
NCT01228864
First Posted: October 27, 2010
Last Update Posted: December 8, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Roswell Park Cancer Institute
  Purpose
The Brody belt may help improve quality of life in patients using urinary drainage bags. PURPOSE: This clinical trial studies the Brody belt in improving the quality of life in patients using urinary drainage bags.

Condition Intervention
Quality of Life Procedure: quality of life Procedure: Quality of life

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Supportive Care
Official Title: Brody Belt - Alternative Method of Securing a Patient's Urinary Drainage Bag

Further study details as provided by Roswell Park Cancer Institute:

Primary Outcome Measures:
  • Quality of Life [ Time Frame: 4 weeks ]

Enrollment: 12
Actual Study Start Date: September 22, 2009
Study Completion Date: August 15, 2017
Primary Completion Date: August 15, 2017 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Brody Belt Procedure: quality of life
survey
Active Comparator: Conventional Urinary Drainage bag Procedure: Quality of life

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

->18 years old

-All patients in the urology clinic at Roswell Park who currently use a urinary drainage bag for a period of at least 7 days prior to signing consent for the study and who are expected to use a urinary drainage tube for an additional period of 4 weeks or more based on the diagnosis

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01228864


Locations
United States, New York
Roswell Park Cancer Institute
Buffalo, New York, United States, 14263
Sponsors and Collaborators
Roswell Park Cancer Institute
Investigators
Principal Investigator: Khurshid Guru, MD Roswell Park Cancer Institute
  More Information

Responsible Party: Roswell Park Cancer Institute
ClinicalTrials.gov Identifier: NCT01228864     History of Changes
Other Study ID Numbers: I 153209
First Submitted: October 25, 2010
First Posted: October 27, 2010
Last Update Posted: December 8, 2017
Last Verified: December 2017