Anti-inflammatory H1 Antihistamines Allergic Rhinitis

Iuliu Hatieganu University of Medicine and Pharmacy

Status and phase: Completed; Phase 4

Conditions: Allergic Rhinitis

Treatments: Drug: Levocetirizine; Drug: Desloratadine

Study type: Interventional

Funder types: Other

Identifiers

NCT02507635

535

Details and patient eligibility

About

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.

Full 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

Enrollment: 115 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• persistent allergic rhinitis

Exclusion criteria

• the presence of asthma or nasal polyps,
• acute and chronic upper respiratory infections,
• administration of intranasal or systemic corticosteroids or H1 antihistamines in the past 30 days.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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115 participants in 3 patient groups

healthy volunteers

No Intervention group

Description:

healthy volunteers

Desloratadine

Active Comparator group

Description:

patients with allergic rhinitis under treatment with Desloratadine 5 mg/day, 4 weeks

Treatment:

Drug: Desloratadine

Levocetirizine

Active Comparator group

Description:

patients with allergic rhinitis under treatment with Levocetirizine 5 mg/day, 4 weeks

Treatment:

Drug: Levocetirizine