Study Results
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View full resultsBasic Information
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COMPLETED
PHASE3
301 participants
INTERVENTIONAL
2009-06-30
2010-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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SER120
SER120
SER120
SER120
Placebo
Placebo
Placebo
Interventions
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SER120
SER120
Placebo
Placebo
Eligibility Criteria
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Inclusion Criteria
* Nocturia of 6 or more months duration averaging 2 episodes or more per night
Exclusion Criteria
* Diabetes
* Diabetes Insipidus
* Renal Insufficiency
* Hepatic Insufficiency
* Incontinence
* Illness requiring steroids
* Current or past urologic malignancy
* Nephrotic Syndrome
* Unexplained pelvic masses
* Urinary bladder neurological dysfunction
* Urinary bladder surgery or radiotherapy
* Sleep Apnea
* Pregnant or breast feeding
50 Years
ALL
No
Sponsors
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Serenity Pharmaceuticals, Inc.
INDUSTRY
Responsible Party
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Locations
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Piedmont Medical Research Assoc.
Winston-Salem, North Carolina, United States
Countries
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Other Identifiers
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SPC-SER120-DB1-200901
Identifier Type: -
Identifier Source: org_study_id
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