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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01740466
Other study ID # Epidemiological public profile
Secondary ID
Status Completed
Phase N/A
First received November 30, 2012
Last updated December 6, 2012
Start date March 2012
Est. completion date August 2012

Study information

Verified date December 2012
Source Instituto de Olhos de Goiania
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Observational [Patient Registry]

Clinical Trial Summary

Epidemiological study about eye discomfort complaints, comorbidities and diagnosis at a Brazil`s ophthalmological public care service


Description:

1. 1670 individuals underwent an ophthalmologic evaluation

2. The data were obtained through the analysis of the medical records with the ICD-10 registration

3. The studied variables were age and sex of patient, origin, eye discomfort complaints, comorbidities and diagnosis (ICD-10).

4. The purpose was to evaluate epidemiological aspects of eye diseases in a public service


Recruitment information / eligibility

Status Completed
Enrollment 1670
Est. completion date August 2012
Est. primary completion date July 2012
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients assisted in public service

Exclusion Criteria:

Study Design

Observational Model: Ecologic or Community, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Brazil Instituto de Olhos de Goiania Goiania Goias

Sponsors (1)

Lead Sponsor Collaborator
Instituto de Olhos de Goiania

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence and prevalence of visual conditions in the Public Service in Brazil The ages ranged from 0 to 99 years
The mean age was 56.9 years
There was a predominance of females (58.1%)
The main reason for the consultation was low visual acuity (70%), followed by burning (26%) and itchiness (24.4%)
Among the abnormal tests there was a high prevalence of refractive errors (73.4%) and presbyopia (59.6%)
The cause of refractive errors was astigmatism (70.5%), hypertrophy (58.6%) and myopia (15.1%)
6 months Yes
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