Sinusitis Clinical Trial
— SNS01Official title:
Non-interventional Study: Application of Ectoin® Rhinitis Nasal Spray in Patients With Acute Rhinosinusitis
Verified date | September 2012 |
Source | Bitop AG |
Contact | n/a |
Is FDA regulated | No |
Health authority | Germany: Federal Institute for Drugs and Medical Devices |
Study type | Observational |
This is a comparative, open label, parallel group, non interventional study to further demonstrate the effectiveness and tolerability of Ectoin® Rhinitis Nasal Spray. In addition the effectiveness and safety shall be compared to a Sinupret forte. The patient applies Ectoin® Rhinitis Nasal Spray or takes Sinupret forte according to the instructions for use. The observation takes place over a period of 14 days. Response to treatment is recorded at day 7 and day 14 by the physician and in daily by the patient in a dairy.
Status | Completed |
Enrollment | 66 |
Est. completion date | August 2012 |
Est. primary completion date | August 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Female or male individuals = 18 years - Patients with acute Rhinosinusitis which are treated with Ectoin® Rhinitis Nasal Spray or Sinupret forte during the observational period Exclusion Criteria: - Contra indications according to the label |
Observational Model: Case-Only, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Germany | Dr. med. Georg Krueckels | Aachen | |
Germany | Dr. med. Martin Sondermann | Aachen | |
Germany | Dr. med. Norbert Pasch | Aachen | |
Germany | Dr. med. Wilhelm Schuetz | Juelich | |
Germany | Peter Hinterkausen | Koeln | |
Germany | Taufik Shahab | Koeln |
Lead Sponsor | Collaborator |
---|---|
Bitop AG |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in the symptoms of acute Rhinosinusitis assessed by the EPOS- Sinusitis-Symptom-Score | day 1, day 7, day 14 | No | |
Secondary | Quality of Life questionnaire (Rhino QoL) | day 1, day 7, day 14 | No | |
Secondary | Rhinoscopy | day 1, day 7, day 14 | No | |
Secondary | Patient's and physician's judgment of efficacy | day 7, day 14 | No |
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