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Clinical Trials/JPRN-UMIN000005012
JPRN-UMIN000005012
Completed
未知

Evaulation of the clinical efficacy and safety of the combined administration of Imidafenacin and Tamsulosin in BPH patients (in which OAB symptoms remain) who did not respond to alpha-1 blocker monotherapy. - Addition Study

Department of Urology, University of Yamanashi, School of Medicine0 sites300 target enrollmentFebruary 4, 2011

Overview

Phase
未知
Intervention
Not specified
Conditions
Overactive bladder
Sponsor
Department of Urology, University of Yamanashi, School of Medicine
Enrollment
300
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 4, 2011
End Date
October 1, 2012
Last Updated
2 years ago
Study Type
Interventional
Sex
Male

Investigators

Sponsor
Department of Urology, University of Yamanashi, School of Medicine

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\)Patients who have administered prohibited substances or who have administered prohibited therapy in the 8 weeks prior to the 1st period (2\)Patients who changed the dosage or usage of a restricted medicine in the specified period before the 1st period (3\)Patients with anuresis (4\)Patients with prostate cancer, neurogenic bladder, urethra stricture, chronic prostatitis, symptomatic urinary tract infection, urinary tract stones and interstitial cystitis (5\)Patients with serious cardiac disorder, serious liver dysfunction and serious kidney dysfunction (6\)Patients with orthostatic hypotension (7\)Patients with pyloristenosis,constriction of dodecadactylon, construction of enteron and adynamic ileus (8\)Patients with deterioration of enterokinesis (9\)Patients with angle\-closure glaucoma (10\) Patients with myasthenia gravis. (11\) Patients in which it has been confirmed that Qmax is less than 5mL/s. (12\)Patients with Polyuria. (13\)Any other patients who are regarded as unsuitable for this study by the investigator

Outcomes

Primary Outcomes

Not specified

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