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Non Interventional Study (NIS) Regarding the Application of Ectoin Mund- & Rachenspray in Patients With Acute Laryngitis and/or Acute Pharyngitis

NCT02160912 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 95

Last updated 2015-01-09

No results posted yet for this study

Summary

In this observational study insights regarding the tolerability and influence on the quality of life of the topical treatment Ectoin Mund- and Rachenspray compared to Emser Pastillen in patients with acute Pharyngitis/ Laryngitis under real life conditions shall be gained.

Patients are treated with Ectoin Mund- \& Rachenspray 1% or Emser Pastillen according to the demands of the physician and the instructions for use.

Conditions

  • Acute Pharyngitis
  • Acute Laryngitis

Sponsors & Collaborators

  • Bitop AG

    lead INDUSTRY

Principal Investigators

  • Ralph Mösges, MD · Klinikum der Universität zu Köln

Eligibility

Min Age
6 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-02-28
Primary Completion
2014-07-31
Completion
2014-12-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02160912 on ClinicalTrials.gov