Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02059018
Other study ID # HypNOCOX-2
Secondary ID 1-10-72-14-14
Status Completed
Phase N/A
First received February 7, 2014
Last updated August 17, 2015
Start date February 2014
Est. completion date August 2015

Study information

Verified date January 2014
Source University of Aarhus
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

The primary objective is to study if a stimulation of nitric oxide and/or prostaglandin affect the diameter changes of retinal vessels during hypoxia. Diameter changes are studied using the Dynamic Vessel Analyzer.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date August 2015
Est. primary completion date February 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- Age between >19 and <61 years

- No known systemic or ocular diseases

Exclusion Criteria:

- Cardio-vascular disease

- Lung disease

- Epilepsy

- Previous ocular disease

- Previous treatment with medications influencing the intraocular pressure or the metabolism of nitric oxide or prostaglandins

- Daily intake of medicine except contraceptive pills

- Pregnancy or breastfeeding

- Known allergy against any of the drugs used in the interventions

Study Design

Allocation: Non-Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Drug:
COX-inhibitor
Administration of 1 drop voltaren 45 minutes before recordings of diameter changes of retinal vessels are initiated
Nitroglycerin
Oral administration of tablet nitroglycerin 0,5mg 5 minutes before recordings of diameter changes of retinal vessels are initiated
COX-inhibitor + Nitroglycerin
Combination of COX-inhibitor and nitroglycerin interventions.

Locations

Country Name City State
Denmark Department of Ophtalmology, Aarhus University Hospital 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 changes of retinal vessels Comparing the differences of diameter changes occuring during each of interventions Examination day 1 and 2 No