Status:
UNKNOWN
Efficacy Maxinom® And Maxitrol® in Reducing The Signs And Symptoms Of Acute Bacterial Conjunctivitis
Lead Sponsor:
Azidus Brasil
Conditions:
Bacterial Conjunctivitis
Acute
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
The primary objective of this study is to evaluate, through clinical parameters, the effectiveness of your medicine topic Maxinom ® (dexamethasone, neomycin and polymyxin B - Union Chemicals), compari...
Detailed Description
1. Evaluation of isolated signs and symptoms during treatment, with a record of individual scores for each parameter and observation 2. Statistical comparison of drug safety, by recording qualitative ...
Eligibility Criteria
Inclusion
- Patients who agree with all study procedures and sign, by his own free will, IC;
- Adult patients, regardless of gender, ethnicity or social status, with good mental health;
- Patients who present at screening visit, picture of acute bacterial conjunctivitis diagnosed clinically.
Exclusion
- Patients with clinical diagnosis or suspicion of conjunctivitis due to any process that is not due to bacterial infection, such as infections by fungi, protozoa, viruses and allergic conjunctivitis;
- Patients with known hypersensitivity to any component of the formulas of the study drugs;
- Patients with a history or clinical diagnosis of other lesions that may affect the outcome, such as glaucoma, corneal ulcer or scars;
- Concomitant use of ocular medication other than the study;
- Pregnant or lactating women;
- Being or having been treated for any type of conjunctivitis within 15 days and have finished treatment or less than 07 days
Key Trial Info
Start Date :
February 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT01227863
Start Date
February 1 2011
Last Update
October 25 2010
Active Locations (1)
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1
LAL Clinica Pesquisa e Desenvolvimento Ltda
Valinhos, São Paulo, Brazil