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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

Conditions
healthy persons
Registration Number
EUCTR2006-001783-23-AT
Lead Sponsor
RSAPHARM Arzneimittel GmbH & Co. KG
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
16
Inclusion Criteria

healthy persons
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Symptoms of any systemic disease, abuse of medications, beverages or drugs

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: Effect of moxaverine in comparison to placebo on ocular blood flow;Secondary Objective: no;Primary end point(s): Retinal, choroidal and optic nerve head blood flow
Secondary Outcome Measures
NameTimeMethod
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