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
- 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: