Clinical Trials Directory

Trials / Completed

CompletedNCT01555736

Comparison of Perennial and Preseasonal Subcutaneous Immunotherapy

A Randomised Double-blind Clinical Trial for Evaluation of Efficacy and Safety of Perennial in Comparison to Preseasonal Grass/Rye Pollen Immunotherapy in Patients Suffering From Seasonal Allergic Rhinitis

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Medical University of Lodz · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Specific immunotherapy, which involves the administration of allergic extracts to patients with symptoms of allergic disorder, is the leading therapeutical tool of modern allergology. According to the latest studies immunotherapy not only reduces symptoms' severity but also may modify the course of allergic disease by reducing the risk of new sensitisations and development of more advanced stages of the disease.It has been hypothesized basing on clinical observation that perennial immunotherapy is more effective and safer in comparison to preseasonal immunotherapy. The aim of the study was to compare the effect of perennial and preseasonal immunotherapy on rhinoconjunctivitis symptoms and safety of both treatments.

Conditions

Interventions

TypeNameDescription
DRUGgrass (80%) and rye (20%) pollens allergoidscomparison of two schemes of immunotherapy - preseasonal and perennial immunotherapy.

Timeline

Start date
2003-01-01
Primary completion
2006-07-01
Completion
2006-09-01
First posted
2012-03-15
Last updated
2012-03-21

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT01555736. Inclusion in this directory is not an endorsement.