Intraocular Pressure (IOP) and Isometric Exercise

NCT ID: NCT00635180

Last Updated: 2011-07-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

9 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-01-31

Study Completion Date

2008-02-29

Brief Summary

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

Detailed Description

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Conditions

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Intraocular Pressure

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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1

1: Healthy subjects

Group Type EXPERIMENTAL

isometric exercise

Intervention Type BEHAVIORAL

Interventions

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isometric exercise

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Young, healthy subjects

Exclusion Criteria

* Known ocular diseases
* Previous ocular trauma
Minimum Eligible Age

18 Years

Maximum Eligible Age

28 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ullevaal University Hospital

OTHER

Sponsor Role lead

Responsible Party

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UllevÄl University Hospital

Principal Investigators

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Sven O Semb, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Ullevaal University Hospital

Locations

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Eye dpt, Ullevaal University Hospital

Oslo, Oslo County, Norway

Site Status

Countries

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Norway

Other Identifiers

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UUS-IOP-07

Identifier Type: -

Identifier Source: org_study_id

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