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

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Bitop

Status

Completed

Conditions

Acute Laryngitis
Acute Pharyngitis

Study type

Observational

Funder types

Industry

Identifiers

NCT02160912
EctMRS/aLR/2014

Details and patient eligibility

About

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.

Enrollment

95 patients

Sex

All

Ages

6+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with acute Laryngitis and/or Pharyngitis which are already treated with Ectoin Mund- & Rachenspray 1% or Emser Pastillen

Exclusion criteria

  • contraindications according to instructions for use

Trial design

95 participants in 2 patient groups

Ectoin Mund- & Rachenspray
Description:
treatment with Ectoin Mund- \& Rachenspray 1%
Emser Pastillen
Description:
treatment with Emser Pastillen

Trial contacts and locations

8

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Data sourced from clinicaltrials.gov

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