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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00619034
Other study ID # 2007-001697-84
Secondary ID XAVOT
Status Completed
Phase N/A
First received February 7, 2008
Last updated December 28, 2010
Start date September 2007
Est. completion date December 2010

Study information

Verified date December 2010
Source University of Aarhus
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if diabetic retinopathy can be treated with prostaglandin analogues, prostaglandin synthesis inhibitors or carbonic anhydrases inhibitors.


Description:

Disturbances in retinal perfusion is believed to be involved in the pathophysiology of diabetic retinopathy. These disturbances may be due to changes in the basal diameter of retinal arterioles and to disturbances in the autoregulation of the diameter of these vessels when the blood pressure and the retinal metabolism changes. In vitro studies have shown that prostaglandins and carbonic anhydrases inhibitors are involved in the tone regulation of retinal arterioles, but it is unknown whether this finding is relevant in clinical practice. This can be tested in vivo by an retinal vessel analyzer measuring the dynamics of the retinal vessel diameter changes.


Recruitment information / eligibility

Status Completed
Enrollment 87
Est. completion date December 2010
Est. primary completion date December 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 35 Years
Eligibility Inclusion Criteria:

- Diabetes type 1 with moderate diabetic retinopathy/healthy

- Blood pressure < 135/85 mmHg

Exclusion Criteria:

- Eye disease (excluding diabetic retinopathy)

- Allergic

- Kidney disease

- Liver disease

- Severe asthma

- Heart disease

- Hypertension arterial

- Users of drugs that influence the metabolism of the prostaglandins in the carbon dioxide

- Pregnant and breastfeeding women and women who don't use secure contraception

- Persons who can't do without contact lens in the treated eye.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Latanoprost, diclofenac and dorzolamide (eyedrops)
1 eyedrop twice daily in one week
Diclofenac
dicolfenac eyedrops twice daily i one eye
Dorzolamide
dorzolamide eyedrops twice daily, in one eye for one week

Locations

Country Name City State
Denmark Department of Ophthalmology Aarhus

Sponsors (1)

Lead Sponsor Collaborator
University of Aarhus

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diameter of retinal blood vessels one year
Secondary Influence on retinal blood flow in diabetes one year
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