Clinical Trials Directory

Trials / Completed

CompletedNCT02507635

Anti-inflammatory H1 Antihistamines Allergic Rhinitis

In Vivo Anti-inflammatory Effect of H1 Antihistamines in Allergic Rhinitis

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
115 (actual)
Sponsor
Iuliu Hatieganu University of Medicine and Pharmacy · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The main purpose of the treatment of persistent allergic rhinitis is to improve symptoms and patients' quality of life and prevent the development of asthma. Therapeutic strategies also target a reduction of pro-inflammatory mediators released from activated cells, including mast cells and epithelial cells. The presence of allergic inflammation in nasal mucosa may increase the risk of asthma occurrence, especially in patients with persistent allergic rhinitis. H1 antihistamines are widely recommended in all types of allergic rhinitis, regardless of symptom severity or persistence. They control all of the symptoms, but to a lesser extent nasal congestion. New generation agents, such as levocetirizine and desloratadine, possess anti-inflammatory properties, reducing allergic inflammation.

Detailed description

Allergic rhinitis is characterized by a chronic inflammation of nasal mucosa and represents a risk factor for asthma occurrence. H1 antihistamines reduce the rhinitis' symptoms, but some compounds may have anti-inflammatory properties. We evaluated the plasmatic level of some cytokines in patients with persistent allergic rhinitis (PAR) and their evolution after 4-week treatment with H1 antihistamines and the risk of asthma after 1.5 year. Eighty-five patients with PAR and 30 healthy volunteers were included in the study. The patients with PAR were randomly divided into 2 groups: 41 patients treated with desloratadine 5 mg/day and 44 patients under levocetirizine 5 mg/day for 4 weeks. The clinical evaluation include the presence and severity of allergic rhinitis' symptoms: rhinorrhea, nasal congestion, sneezing, nasal and ocular itching and duration of the disease. Each symptom was evaluated on scale from 0 to 3 (0=absent, 1=mild, 2=moderate, 3=severe) and after that we calculated the total symptoms score (TSS). A TSS\<6 means a mild rhinitis, while a TSS\> 6 represented a moderate severe one. The patients were clinically evaluated after 1.5 year to determine the possible onset of bronchial asthma. The biological evaluation means determination of total IgE and plasmatic level of IL-1 beta, IL-6, IL-8 and TNF alpha. Clinical and biological evaluation were performed before and after treatment

Conditions

Interventions

TypeNameDescription
DRUGLevocetirizineadministration of Levocetirizine 5 mg/day for 4 weeks
DRUGDesloratadineadministration of Desloratadine 5 mg/day for 4 weeks

Timeline

Start date
2009-02-01
Primary completion
2011-11-01
Completion
2013-05-01
First posted
2015-07-24
Last updated
2015-07-24

Source: ClinicalTrials.gov record NCT02507635. Inclusion in this directory is not an endorsement.