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Efficiency of phototherapy in management of patients with allergic rhinitis

Phase 2
Conditions
Allergic Rhinitis.
Allergic rhinitis due to pollen
Registration Number
IRCT2015042621944N1
Lead Sponsor
Vice chancellor for Research, Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
64
Inclusion Criteria

Inclusion Criteria:1-Men and women 18 – 60 years of age; 2-Out-patients, with a history and diagnosis of allergic rhinitis for at least two years prior to Visit 1; 3-Allergy verified by a positive skin-prick test or specific IgE determination within two years prior to visit 1, or at visit 1; 4-Patients have allergic rhinitis with no response to previous local or systemic antihistamines/corticosteroids, or patients do not want these therapeutic measures or can 't be treated with these drugs due to side effects or any other reasons; 5-Patients having severe disease, where the global severity score was more than 6 in the 10 point scale in the last 3 days before enrollment; 6-Signed Informed Consent obtained from the patient prior to conducting any study-related procedures;

Exclusion Criteria

1-Known light-induced skin disease (photodermatosis); 2-Ongoing fungal, viral or bacterial respiratory infection; 3-Anatomic abnormalities in the nose (eg: severe septum deviation or polyps) that disturb photo therapeutically treatment, as judged by the Investigator; 4-Prohibited Medicines such as Digoxin, Doxepin, Amiodarone, Trimethoprim , Chlorpropamide, Piroxicam, Doxycycline, Promethazine all can cause photosensitivity and Wash-Out Periods for PHOTO-SENSITIZING MEDICATIONS (eg: Systemic corticosteroids: 4 weeks; Intranasal Cromolyn, Intranasal and topical corticosteroids: 2 weeks; Intranasal decongestants: 3 days; Intranasal or systemic antihistamines: 1 week; Immunotherapy: 5 years) before beginning the study; 5-Patients less than 18 years old; 6-Pregnant women; 7-Patients unable to give informed consent because of age, mental illness, dementia or communication difficulties and patients with nasopharyngeal tumors all are excluded.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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