CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 123 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01660737
NCT01660737N/ACompleted

Observational Study With PASCALLERG ® in Patients With Hay Fever

Pascoe Pharmazeutische Praeparate GmbH·observational·Posted Aug 9, 2012·Updated Mar 30, 2021

In Brief

An observational study for Hay Fever. Completed, enrolled 123 participants across 1 site.

Detailed Summary

The aim of this observational study is to document the therapeutic use of PASCALLERG ® for hay fever. Based on the survey is a decrease in disease-specific symptoms when taking PASCALLERG ® over a period of 4 weeks will be documented. In addition to the compatibility can be assessed.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsHay Fever
CountriesGermany
Collaborators--

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedAug 9, 2012
Enrollment StartFeb 1, 2012
Primary CompletionJul 1, 2013
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 13.9 years ago