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Clinical study of subcutaneous immunotherapy dose adjustments in the treatment of allergic rhinitis

Clinical study of subcutaneous immunotherapy dose adjustments in the treatment of allergic rhinitis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000033808
Enrollment
Unknown
Registered
2020-06-13
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Allergic rhinitis

Interventions

the control group:adopting referenced dose adjustment schedule
the experimental group:adopting new dose adjustment schedule

Sponsors

The First People's Hospital of Foshan
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients aged 5-60 years; 2. Patients with typical ar history and clinical symptoms of intermittent or persistent paroxysmal sneezing, clear water like snot, rhinopruritus and nasal obstruction; 3. The specific IgE of house dust mite and dust mite allergen in skin prick test was >= 0.70 Ku / L; 4. Patients with delayed injection in the routine subcutaneous immunotherapy of "Arog".

Exclusion criteria

Exclusion criteria: 1. Pregnant and lactating women; 2. Patients with severe or uncontrolled asthma (FEV1 < 70% of predicted value) and irreversible respiratory obstructive diseases; 3. Patients with hypertension and coronary heart disease who are not suitable for adrenaline treatment; 4. Patients with severe immune diseases; 5. Patients with severe psychological disorders, or unable to understand the risks and limitations of treatment; 6. Patients with malignant tumors.

Design outcomes

Primary

MeasureTime frame
severe local reaction;systemic reaction;satisfaction scores;

Secondary

MeasureTime frame
symptom score;medication score;life quality score;

Countries

China

Contacts

Public ContactQingqing Yu

The First People's Hospital of Foshan

tommyair123@163.com+86 18038860196

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026