Status:
COMPLETED
ADenoVirus Initiative Study in Epidemiology in Spain
Lead Sponsor:
NicOx
Conditions:
Viral Conjunctivitis
Eligibility:
All Genders
1+ years
Brief Summary
The objectives of this study is to assess the characteristics and frequency of adenovirus conjunctivitis in a population of male and female patients from one year of age who present signs and symptoms...
Detailed Description
Epidemiological, prospective, open, multicentric trial in patients suffering from acute conjunctivitis who will undergo a rapid diagnostic test for adenoviral conjunctivitis at the time of their visit...
Eligibility Criteria
Inclusion
- Male or Female patients of at least one year of age presenting acute (for less than 7 days) conjunctivitis signs and symptoms.
- Patient or / and legal representative (if patient below 18 years of age) must be able to provide oral consent for the collection and treatment of the questionnaire data.
- No history of hypersensitivity to corn starch, talcum powder or Dacron (sampling fleece components).
Exclusion
- Current use or having received (within the last 7 days) local antiviral therapies such as povidone iodine or ganciclovir, or topical steroids or immunomodulators such as cyclosporine which may interfere with the test result.
- Previous enrolment in the present study.
- Any direct involvement with the study conduct at site or any family link with study site staff.
Key Trial Info
Start Date :
July 1 2014
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
August 1 2015
Estimated Enrollment :
386 Patients enrolled
Trial Details
Trial ID
NCT02254330
Start Date
July 1 2014
End Date
August 1 2015
Last Update
January 10 2017
Active Locations (25)
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1
VISSUM
Alicante, Spain
2
Clinica Barraquer
Barcelona, Spain
3
Hospital Clinic
Barcelona, Spain
4
Instituto de Microcirugía Ocular
Barcelona, Spain