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Completed

NCT Number: NCT05753241

the Relationship Between Allergic Rhinitis and the Risk of Symptom in Patients With Mild COVID-19

At present, most studies mainly focussed on severe patients, and there was no comparison of symptom differences between AR patients and healthy people with mild infection to evaluate the symptoms of AR patients during infection and to provide preventive treatment in advance. So this experiment was designed.

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Key information

About this study

After the end of this large-scale infection, the investigators analyzed the re-diagnosis of patients with allergic rhinitis (AR) at the Otolaryngology Clinic, and found significant differences in symptoms between AR and non-AR patients. AR patients had more serious nasal and pharyngeal symptoms. In previous studies on the correlation between allergic diseases and COVID-19 infection, AR was found to be a protective factor to reduce COVID-19 infection and the risk of severe disease . In contrast, a cohort study in South Korea found that AR worsened COVID-19 infection . These studies mainly focussed on severe patients, and there was no comparison of symptom differences between AR patients and healthy people with mild infection.

Allergy may lead to the overall damage of nasal mucosa due to the mechanical and immune defense function of the virus. Immunotherapy will significantly reduce the number and severity of upper respiratory tract infections (including children's common cold). The investigators hypothesized that AR is more likely to aggravate symptoms after infection, while allergen immunotherapy (AIT) may reduce the risk of symptoms as a protective factor for symptoms after AR virus infection. Therefore, the investigators conducted a retrospective analysis on the risk of symptoms after COVID-19 infection in patients with AR, and compared the difference of symptoms after COVID-19 infection in patients with AIT and non-AIT AR.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • all participants completed at least one antigen or nucleic acid test and the results were positive.
  • the diagnoses of AR met the international diagnostic standards for AR. The participants had obvious clinical symptoms and the allergen test was positive.

Exclusion criteria

  • suspected new infected person with symptoms( no antigen or nucleic acid test and the results were nagetive )
  • Participants requiring ICU admission after COVID-19 infection-

Treatment and study plan

No intervention

Other

It's only observational study. No interventions.

Primary outcomes

  1. post-infection symptoms(pharyngeal symptoms;Systemic symptoms; Gastrointestinal symptoms;Olfactory and gustatory dysfunction;Severe symptoms)

    Time frame: The first day after COVID-19 infection

    pharyngeal symptoms: dry throat, itchy throat, sore throat, cough, expectoration; Systemic symptoms: fever, headache, fatigue, cold limbs; Gastrointestinal symptoms: diarrhea, constipation; Olfactory and gustatory dysfunction: hypoosmia, hypogustia; Severe symptoms: chest tightness, pant, palpitation, convulsion, coma.

  2. hospitalization rate

    Time frame: The first day after COVID-19 infection

    The probability of needing hospital treatment after infection

Sponsors and collaborators

Lead sponsor

qinxiu zhang

Other

Registry information

Official study title

Hospital of Chengdu University of Traditional Chinese Medicine

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Mar 3, 2023
Registry last updated
Mar 1, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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