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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT00569621 |
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Date of registration:
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05/12/2007 |
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Primary sponsor: |
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Public title:
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A Randomized, Double-Masked, Placebo-Controlled Two Cross Over Study Comparing the Effects of Moxaverine and Placebo on Ocular Blood Flow
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Scientific title:
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A Randomized, Double-Masked, Placebo-Controlled Two Cross Over Study Comparing the Effects of Moxaverine and Placebo on Ocular Blood Flow |
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Date of first enrolment:
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March 2007 |
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Target sample size:
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16 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00569621 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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Countries of recruitment
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Austria
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Contacts
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Name:
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Michael Wolzt, Prof |
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Address:
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Telephone:
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Email:
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Affiliation:
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Department of Clinical Pharmacology |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- 6 healthy volunteers of either sex
- Age 18-35 yrs.
- Body mass index between 15th and 85th percentile, nonsmokers
Exclusion Criteria:
- Regular use of medication
- Abuse of alcoholic beverages or drugs
- Participation in a clinical trial in the 3 weeks preceding the study
- Treatment in the previous 3 weeks with any drug
- Symptoms of a clinically relevant illness in the 3 weeks before the first study day
- History or presence of gastrointestinal, liver or kidney disease, or other conditions known to interfere with distribution, metabolism or excretion of study drugs
- Blood donation during the previous 3 weeks
- Ametropy less 3 dpt
- Acute gastric bleeding, massive cerebral hemorrhage related to stroke
- Women: pregnancy or lactation.
Age minimum:
18 Years
Age maximum:
35 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Ischemia
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Intervention(s)
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Drug: Moxaverine
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Drug: physiological saline
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Primary Outcome(s)
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Retinal and Choroidal Blood flow
[Time Frame: 2 hours]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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