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NOT YET RECRUITING
NCT07625683

Observational Study of SIROPSEDAL in Acute Cough

Sponsor: Laboratoires Elerte

View on ClinicalTrials.gov

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