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Observational Study of SIROPSEDAL in Acute Cough
Sponsor: Laboratoires Elerte
Summary
This prospective, multicenter, observational post-market clinical follow-up study evaluates the performance and safety of SIROPSEDAL in children and adults with acute cough treated in routine clinical practice. Patients prescribed SIROPSEDAL independently of study participation will be followed for 7 +/- 1 days using patient-reported outcomes including a cough visual analog scale and the Cough Symptom Score.
Official title: Prospective Multicenter Before-After Study in Children and Adults Treated for Acute Cough With SIROPSEDAL
Key Details
Gender
All
Age Range
1 Year - Any
Study Type
OBSERVATIONAL
Enrollment
124
Start Date
2026-10-15
Completion Date
2027-09-30
Last Updated
2026-06-04
Healthy Volunteers
No
Locations (1)
Multiples facilities
Multiple Locations, France