Expired Study
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Los Angeles, California 90095


Purpose:

Crossover comparison of different flow meters with a digital home flow meter as a reference. Main hypothesis: Reapeated home flow measurements with CaptiFlow will provide a better understanding of the patients urinary flow than a single measurement performed in the clinic.


Criteria:

Inclusion Criteria: - Provision of informed consent - Males aged 45-85 years - >60% of the voiding volume is above 100 ml per voiding verified by a urinary diary - Able to read write and understand given instructions Exclusion Criteria: - Patients practicing CIC - Ongoing symptomatic UTI - Known Neurological Disease that is affecting the bladder function - Known past or present alcohol or drug abuse - Involvement in the planning and conduct of the study (applies to both Astra Tech staff or staff at the study site) - Previous enrolment or randomisation of treatment in the present study. - Suspected poor compliance based on less than 80 % compliance to voiding diary - Severe non-compliance to protocol as judged by the investigator and/or Astra Tech - On alpha-blocker or 5-alpha reductase inhibitor treatment, treatment started less than 2 months prior to enrolment - Clinic flow below 100 ml


NCT ID:

NCT00710749


Primary Contact:

Study Chair
Magnus Jacobsson, Prof.
Astra Tech AB


Backup Contact:

N/A


Location Contact:

Los Angeles, California 90095
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 23, 2018

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