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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02131038
Other study ID # Rep-25
Secondary ID
Status Completed
Phase N/A
First received April 25, 2014
Last updated May 5, 2014
Start date May 2009
Est. completion date September 2009

Study information

Verified date May 2014
Source Bitop AG
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Observational

Clinical Trial Summary

This is a comparative, open label, parallel group, non interventional study to further demonstrate the effectiveness and tolerability of Ectoin Allergy Nasal Spray. In addition the effectiveness and safety shall be compared to a Cromoglycid acid containing nasal spray. The patient applies Ectoin Allergy Nasal Spray or Cromoglycid acid containing nasal spray 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 by the patient in a dairy at defined time intervalls.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date September 2009
Est. primary completion date September 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Female or male individuals = 18 years

- Patients with proven Allergic Rhinitis which are treated with Ectoin Nasal Spray or -Cromoglycic acid nasal Spray during the observational period

Exclusion Criteria:

- Contra indications according to the label

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Medica device, drug-like
Ectoin (R) Allergy Nasal Spray

Locations

Country Name City State
Germany HNO Praxis Elmshorn Elmshorn

Sponsors (1)

Lead Sponsor Collaborator
Bitop AG

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in combined nasal symptom Score The change in the sum of the three different parameters nasal congestion, rhinorrhea and nasal errhine were investigated as combined score. Time Frame: day 1, day 7, day 14 No
Secondary Patient's and physician's judgment of efficacy Patient and physician were asked to grade the efficacy of the treatment on a scale from 0 to 8. Day 7 and 14 No
Secondary Eye itching score, Day 1, 7, 14 No
Secondary Epiphora score Day1, Day 7 and Day 14 No
Secondary Conjunctivitis score, Day 1, Day 7 Day 10 No
Secondary Palatal itching score Day 1, Day 7, Day 14 No
Secondary Nasal muscle hyperplasia score Day 1, Day 7 and Day 14 No
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