Comparative Study Between Tonometers

Sponsor
Instituto de Olhos de Goiania (Other)
Overall Status
Completed
CT.gov ID
NCT03338101
Collaborator
(none)
100
1
4
25.2

Study Details

Study Description

Brief Summary

Comparative study between the Goldmann Flattening Tonometer and the Non-Contact Tonometer in patients of a Reference Ophthalmological Hospital

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    100 participants
    Observational Model:
    Ecologic or Community
    Time Perspective:
    Retrospective
    Official Title:
    Comparative Study Between the Goldmann Flattening Tonometer and the Non-Contact Tonometer in Patients of a Reference Ophthalmological Hospital
    Actual Study Start Date :
    Jul 1, 2017
    Actual Primary Completion Date :
    Sep 1, 2017
    Actual Study Completion Date :
    Oct 30, 2017

    Outcome Measures

    Primary Outcome Measures

    1. Comparative study between the Goldmann Flattening Tonometer and the Non-Contact Tonometer in patients of a Reference Ophthalmological Hospital [3 months]

      evaluation of the intraocular pressure

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    1 Year to 100 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Inclusion Criteria:Pacients with glaucoma diagnosed -

    Exclusion Criteria:Pacients without glaucoma diagnosed

    -

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Instituto de Olhos de Goiania GoiĆ¢nia Goias Brazil 74110120

    Sponsors and Collaborators

    • Instituto de Olhos de Goiania

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Instituto de Olhos de Goiania
    ClinicalTrials.gov Identifier:
    NCT03338101
    Other Study ID Numbers:
    • TRABALHO GLENDA ARVO 2018
    First Posted:
    Nov 9, 2017
    Last Update Posted:
    Nov 9, 2017
    Last Verified:
    Nov 1, 2017
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 9, 2017