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Clinical Trial Details

Trial ID: L1194
Source ID: NCT02033798
Associated Drug: Tamsulosin
Title: The Effect of Daily Tamsulosin 0.2mg Administration on Renal Function in Patients With Benign Prostatic Hyperplasia
Acronym:
Status: UNKNOWN
Study Results: NO
Results:
Conditions: Chronic Kidney Failure|Prostatic Hyperplasia
Interventions: DRUG: Tamsulosin
Outcome Measures: Primary: Maximal flow rate, This parameter can be obtained from urodynamic study., 6 months|Maximal detrusor pressure, This parameter can be obtained from urodynamic study., 6 months|Bladder outlet obstruction index, This parameter can be obtained from urodynamic study., 6 months|schäfer grade, This parameter can be obtained from urodynamic study., 6 months|Compliance, This parameter can be obtained from urodynamic study., 6 months | Secondary: Estimated glomerular filtration rate, 6 months|Urinary protein to creatinine ratio, 6 months | Other: International prostate symptom score, 6 months
Sponsor/Collaborators: Sponsor: The Catholic University of Korea
Gender: MALE
Age: ADULT, OLDER_ADULT
Phases:
Enrollment: 34
Study Type: INTERVENTIONAL
Study Designs: Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2014-02
Completion Date: 2016-06
Results First Posted:
Last Update Posted: 2014-01-17
Locations: St. Vincent's Hospital, Suwon, Gyeonggi-do, 442-723, Korea, Republic of
URL: https://clinicaltrials.gov/show/NCT02033798