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NCT00635180 Clinical Trial

Intraocular Pressure (IOP) and Isometric Exercise

Intraocular Pressure Clinical Trial

Official title:
Changes in Intraocular Pressure and Pulsatile Ocular Blood Flow Measured Continuously During Isometric Exercise

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00635180
Other study ID # UUS-IOP-07
Secondary ID
Status Completed
Phase N/A
First received February 5, 2008
Last updated July 3, 2011
Start date January 2007
Est. completion date February 2008

Study information
Verified date February 2008
Source Oslo University Hospital
Contact n/a
Is FDA regulated No
Health authority Norway:National Committee for Medical and Health Research Ethics
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate changes in intraocular pressure measured continuously during isometric exercise.

Recruitment information / eligibility
Status Completed
Enrollment 9
Est. completion date February 2008
Est. primary completion date March 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 28 Years
Eligibility Inclusion Criteria:

- Young, healthy subjects

Exclusion Criteria:

- Known ocular diseases

- Previous ocular trauma

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science

Related Conditions & MeSH terms

Intervention

Behavioral:
• isometric exercise

Locations
Country Name City State
Norway Eye dpt, Ullevaal University Hospital Oslo

Sponsors (1)
Lead Sponsor Collaborator
Ullevaal University Hospital

Country where clinical trial is conducted

Norway, 

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