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The clinical efficacy, sleep quality of life, and safety of short-course oral corticosteroids for treating children and adolescents coexisting with moderate-to-severe allergic rhinitis and habitual snoring

The clinical efficacy, sleep quality of life, and safety of short-course oral corticosteroids for treating children and adolescents coexisting with moderate-to-severe allergic rhinitis and habitual snoring

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20250218019
Enrollment
60
Registered
2025-02-18
Start date
2025-01-31
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

uncontrolled moderate-to-severe persistent allergic rhinitis and habitual snoring allergic rhinitis, corticosteroids, persistent, sleep-disordered breathing

Interventions

Children aged 2-15 years who had been diagnosed by a physician with moderate-to-severe persistent allergic rhinitis and habitual snoring that was uncontrolled. These patients are given oral corticoste
Treatment

Sponsors

Buddhasothorn Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 15 Years

Inclusion criteria

Inclusion criteria: 1. Children aged 2-15 years who had been diagnosed by a physician with moderate-to-severe persistent allergic rhinitis and habitual snoring that was uncontrolled. 2. The participants have been previously treated with intranasal corticosteroids, antihistamines, and montelukast for at least 2 weeks at standard doses of treatment but have not been able to control their allergic rhinitis symptoms (Visual Analogue Scale for allergic rhinitis > 50).

Exclusion criteria

Exclusion criteria: 1. Patients with a history of allergy to corticosteroids (oral, inhaled, or intranasal). 2. Patients diagnosed with primary or secondary immunodeficiency or receiving immunosuppressant therapy. 3. Patients with upper respiratory tract infection within 2 weeks prior to treatment in this study. 4. Patients who had taken antibiotics within 4 weeks prior to treatment in this study. 5. Patients diagnosed with sinusitis, congenital heart disease, or ECG abnormalities or cardiac arrhythmias; patients with bone and joint disorders, pregnancy, psychiatric disorders, circulatory system diseases, metabolic syndrome, and obese patients. 6. Patients diagnosed with craniofacial abnormalities, neuromuscular diseases, gastroesophageal reflux disease, Down syndrome, bronchial malformations, cardiovascular diseases, and other chronic pulmonary diseases other than asthma. 7. Patients who had taken oral or inhaled corticosteroids in the past 4 weeks before being enrolled in this study. 8. Pediatric patients who are at risk for side effects from corticosteroids, such as those diagnosed with hypertension, diabetes mellitus, high intraocular pressure or glaucoma, cataracts, parasitic infections, chest X-ray results suspected of infectious pneumonia, found red blood cells in the stool, gastrointestinal diseases such as peptic ulcer disease or gastroesophageal reflux disease, or there is an infection in various systems of the body, such as fungus on the skin, nails, or in the mouth, skin disease from infection with the varicella virus.

Design outcomes

Primary

MeasureTime frame
Assessment of disease control in allergic rhinitis at 1-2 weeks after end of the intervention Visual Analogue Scale for allergic rhinitis

Secondary

MeasureTime frame
Assessment of disease control in habitual snoring at 1-2 weeks after end of the intervention Pediatric Sleep Questionnaire (PSQ),Assessment of quality of life at 1-2 weeks after end of the intervention The 18-item obstructive sleep apnea(OSA-18-QOL) questionnaire

Countries

Thailand

Contacts

Public ContactSuttipong Ittiporn

Buddhasothorn Hospital

suttipong.itt@gmail.com0894029802

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026