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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00413751
Other study ID # WRAMC WU #03-23004
Secondary ID
Status Completed
Phase N/A
First received December 19, 2006
Last updated December 19, 2006

Study information

Verified date December 2006
Source Walter Reed Army Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

The objective of this study is to evaluate the effect of brimonidine tartrate ophthalmic solution 0.15% (Alphagan P) on pupil diameter under different luminance conditions.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Adult active duty personnel between 18 and 50 years of age with best corrected visual acuity of 20/20 or better.

Exclusion Criteria:

- Patients not meeting above stated age criteria

- Females that are pregnant or lactating (non pregnant females of childbearing potential will have pregnancy test prior to participating in study)

- History of serious ocular, neurological, cardiovascular disease

- History of severe systemic disease

- History of arrhythmias or high blood pressure

- Patients currently taking any type of ocular or systemic medications except multivitamins.

- Patients with abnormal pupil shape, Addie's pupil, anisocoria, or abnormal pupil defect.

Study Design

Time Perspective: Longitudinal


Related Conditions & MeSH terms


Intervention

Drug:
Brimonidine tartrate ophthalmic solution 0.15% (Alphagan P)


Locations

Country Name City State
United States Walter Reed Army Medical Center Washington District of Columbia

Sponsors (1)

Lead Sponsor Collaborator
Walter Reed Army Medical Center

Country where clinical trial is conducted

United States, 

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