Respiratory Tract Infections Clinical Trial
Official title:
Evaluation of the Treatment With Klacid SR in Patients With Acute Tracheitis, Tracheobronchitis and Bronchitis, Acute Exacerbation of Chronic Bronchitis and Mild Community-acquired Pneumonia in Common Clinical Practice in Ukraine
To describe the relief of symptoms, tolerability, and compliance of treatment with Klacid®
sustained release (SR) at a dose of 1000 mg once daily in patients with acute tracheitis,
acute tracheobronchitis, acute bronchitis, or in patients with acute exacerbation of chronic
bronchitis or mild community-acquired pneumonia.
This postmarketing observational study is non-interventional and is being conducted in a
prospective, single-arm, single-country, multicenter format.
Klacid SR will be prescribed in usual manner in accordance with the terms of the local
market authorization with regards to dose, population, and indication as well as with local
guidelines.
The postmarketing observational study is observational in nature. Its follow-up is not
interventional and is left to the judgment of each physician during the observational
period, which defines the survey for each patient. Follow-up of patients should enable two
patient visits during this period.
The screening/inclusion visit (Visit 1) will be performed when the decision for Klacid SR
therapy in a daily dose of 1000 mg is made. The second visit of the patient will occur 10 -
16 days from the screening/inclusion Visit (upon physician's decision). The physician can
change the numbers and time of the visits. As a result, failure to meet these suggested
dates will not constitute a breach of the protocol.
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Time Perspective: Prospective
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