Effects of Moxaverine and Placebo on Ocular Blood Flow

Phase 2

Completed

• Conditions: Regional Blood Flow; Ocular Physiology; Retina
• Interventions: Drug: Moxaverine; Drug: NaCl; Drug: Moxaverin 150mg

• Registration Number: NCT00709423
• Lead Sponsor: Medical University of Vienna

Brief Summary

A number of common eye diseases such as retinal artery and vein occlusion, diabetic retinopathy, age-related macular degeneration, glaucoma and anterior ischemic optic neuropathy are associated with ocular perfusion abnormalities. Although this is well recognized there is not much possibility to improve blood flow to the posterior pole of the eye in these diseases.

Since many years, moxaverine is used in the therapy of perfusion abnormalities in the brain, the heart and the extremities. This is based on a direct vasodilator effect of the drug, but also on the rheological properties of red blood cells. Whether moxaverine affects blood flow in the eye is unknown. The present study aims to investigate whether moxaverine may improves blood flow in the eye after systemic administration.

Detailed Description

Not available

Study Timeline

• Study Start: 2007-03
• Primary Completion: 2007-05
• Study Completion: 2007-05
• Status Verified: 2008-06
• Study First Submitted: 2008-07-01
• Study First Submitted QC: 2008-07-02
• Last Update Submitted: 2008-07-02
• Study First Posted: 2008-07-03
• Last Update Posted: 2008-07-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 16

Inclusion Criteria

• Men and women aged between 18 and 35 years, nonsmokers
• Body mass index between 15th and 85th percentile
• Normal findings in the medical history and physical examination unless the investigator considers an abnormality to be clinically irrelevant
• Normal laboratory values unless the investigator considers an abnormality to be clinically irrelevant
• Normal ophthalmic findings, ametropy < 3 dpt.

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 >= 3 dpt
• Acute gastric bleeding, massive cerebral hemorrhage related to stroke
• Women: pregnancy or lactation

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
1	Moxaverine	-
1	Moxaverin 150mg	-
2	NaCl	-

Primary Outcome Measures

Name	Time	Method
Retinal blood flow (Laser Doppler Velocimetry, Retinal Vessel Analyzer)	2 hours
Choroidal and optic nerve head blood flow (Laser Doppler Flowmetry)	2 hours

Trial Locations

Locations (1)

Department of Clincal Pharmacology, Medical University of Vienna; 🇦🇹 Vienna, Austria