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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00818233
Other study ID # 0601001047
Secondary ID
Status Withdrawn
Phase N/A
First received November 18, 2008
Last updated May 11, 2016
Start date January 2009

Study information

Verified date May 2016
Source Yale University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The aim of the protocol is to document intra-observer and inter-observer variability with dynamic contour tonometry, and will also test the theory that pulse amplitude, as measured by dynamic contour tonometry, is correlated with the difference in systolic and diastolic blood pressures.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Normal, healthy eyes

- Minimal to moderate refractive error

- Willingness to participate in the study

Exclusion Criteria:

- Diagnosis of any type of glaucoma

- Any prior ocular surgery

- Any prior ocular trauma

- Any known anterior segment pathology

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
Dynamic contour tonometry
Observe variability of measurements by dynamic contour tonometry

Locations

Country Name City State
United States Yale Eye Center New Haven Connecticut

Sponsors (1)

Lead Sponsor Collaborator
Yale University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The variability of intraocular pressure measurements using dynamic contour tonometry Same day No
Secondary Observe how pulse amplitude, as measured by dynamic contour tonometry, correlates with the difference in systolic and diastolic blood pressures Same day No
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