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Changes in nasal obstruction in adolescents with allergic rhinitis after laser use

Effects of photobiostimulation with red and infrared laser on nasal obstruction in adolescents with allergic rhinitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-8ghk566
Enrollment
Unknown
Registered
2023-11-15
Start date
2022-06-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Allergic rhinitis, unspecified

Interventions

This clinical trial has a cross-sectional, randomized, controlled, double-blind crossover clinical trial that will evaluate children and adolescents from the outpatient clinic of the Discipline of All

Sponsors

Escola Paulista de Medicina
Lead Sponsor
Escola Paulista de Medicina
Collaborator

Eligibility

Age
8 Years to 17 Years

Inclusion criteria

Inclusion criteria: Age between 8 and 17 years old, medical diagnosis of RA (ARIA) present in the medical record for at least 12 months; allergic sensitization by immediate reading skin test (Prick test) or specific serum IgE to at least one inhaled allergen in the last 12 months; degree of nasal obstruction with values equal to five on the day of the test on a visual analogue scale (5 to 10).

Exclusion criteria

Exclusion criteria: Severe or uncontrolled asthma; use of topical medication (nasal decongestant in the last 24 hours); topical corticosteroids within two weeks; use of oral medication: systemic corticosteroids within the last four weeks,chromones within d weeks, antihistamines within a week or immunotherapy five years before the start of the study; severe systemic disease; history or signs of upper or lower respiratory infection within the last four weeks; anatomical defects of the upper airways (nasal polyposis, adenoid hypertrophy, deviated septum, tumor mass) documented in the medical record or observed on physical examination; maxillary atresia; history of epistaxis.

Design outcomes

Primary

MeasureTime frame
It is expected to find a mean difference in the parameters evaluated for patient improvement in the state of nasal obstruction after application of laser therapy.

Secondary

MeasureTime frame
No secondary outcomes are expected

Countries

Brazil

Contacts

Public ContactEscola de Medicina

Universidade Federal de São Paulo

diretoria.epm@unifesp.br+55(11)5576-4848

Outcome results

None listed

Source: REBEC (via WHO ICTRP)