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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.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00569621
Date of registration: 05/12/2007
Primary sponsor: Medical University of Vienna
Public title: A Randomized, Double-Masked, Placebo-Controlled Two Cross Over Study Comparing the Effects of Moxaverine and Placebo on Ocular Blood Flow
Scientific title: A Randomized, Double-Masked, Placebo-Controlled Two Cross Over Study Comparing the Effects of Moxaverine and Placebo on Ocular Blood Flow
Date of first enrolment: March 2007
Target sample size: 16
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT00569621
Study type:  Interventional
Study design:  Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment  
Countries of recruitment
Austria
Contacts
Name:   Michael Wolzt, Prof
Address: 
Telephone:
Email:
Affiliation:  Department of Clinical Pharmacology
Key inclusion & exclusion criteria

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
Health Condition(s) or Problem(s) studied
Ischemia
Intervention(s)
Drug: Moxaverine
Drug: physiological saline
Primary Outcome(s)
Retinal and Choroidal Blood flow [Time Frame: 2 hours]
Secondary Outcome(s)
Secondary ID(s)
MOXOPH1
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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