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| Sponsor: | Seoul National University Hospital |
|---|---|
| Information provided by: | Seoul National University Hospital |
| ClinicalTrials.gov Identifier: | NCT00700583 |
Purpose
The aim of the present study was to determine whether the combined administration of a diuretic agent, hydrochlorothiazide, at night would improve the frequency of nocturia unresponsive to alpha-blocker monotherapy in men with LUTS.
| Condition | Intervention |
|---|---|
|
Nocturia |
Drug: combination therapy of terazosin and hydrochlorothiazide |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Alpha-blocker Plus Diuretic Combination Therapy as Second-line Treatment for Nocturia in Men With LUTS: a Pilot Study |
| Enrollment: | 72 |
| Study Start Date: | May 2008 |
| Study Completion Date: | June 2008 |
| Primary Completion Date: | June 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: 1 |
Drug: combination therapy of terazosin and hydrochlorothiazide
25 mg of hydrochlorothiazide eight hours before bedtime and 4 mg of terazosin at bedtime for 4 weeks
|
Because nocturia may result in sleep disturbances, daytime fatigue, a lower level of general well-being, and an increased risk of falling at night, it is among the most bothersome of the lower urinary tract symptoms (LUTS). Nocturia is related to a variety of conditions such as aging, overactive bladder (OAB), benign prostatic hyperplasia (BPH)/LUTS, medications, diabetes mellitus, diabetes insipidus, anorexia nervosa, and sleep disturbance. In a previous study, we suggested that treatment with terazosin can reduce episodes of nocturia, both subjectively and objectively, in some men with LUTS. Other study showed that in men with nocturnal polyuria, furosemide resulted in a significant reduction in night-time frequency and percentage of the voided volume.
Eligibility| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Korea, Republic of | |
| Department of Urology, Seoul National University Hospital | |
| Seoul, Korea, Republic of, 110-744 | |
| Principal Investigator: | Min Chul Cho, M.D. Master | Department of Urology, Seoul National University College of Medicine |
More Information
| Responsible Party: | Jae-Seung Paick/M.D.,Ph.D., Seoul National University Hospital |
| ClinicalTrials.gov Identifier: | NCT00700583 History of Changes |
| Other Study ID Numbers: | mccho |
| Study First Received: | June 16, 2008 |
| Last Updated: | May 9, 2011 |
| Health Authority: | Korea: Food and Drug Administration |
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nocturia bladder urination disorders hydrochlorothiazide terazosin |
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Nocturia Urological Manifestations Signs and Symptoms Adrenergic alpha-Antagonists Terazosin Diuretics Hydrochlorothiazide Adrenergic Antagonists Adrenergic Agents Neurotransmitter Agents |
Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Physiological Effects of Drugs Natriuretic Agents Sodium Chloride Symporter Inhibitors Membrane Transport Modulators Antihypertensive Agents Cardiovascular Agents Therapeutic Uses Adrenergic alpha-1 Receptor Antagonists |