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Application of Ectoin® Rhinitis Nasal Spray in Patients With Acute Rhinosinusitis (SNS01)

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Bitop

Status

Completed

Conditions

Sinusitis

Treatments

Drug: Sinupret forte
Other: Medical Device, Drug-like

Study type

Observational

Funder types

Industry

Identifiers

NCT01684540
NIS SNS01
PPL-047

Details and patient eligibility

About

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.

Enrollment

66 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

6

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Data sourced from clinicaltrials.gov

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