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Clinical study of stem cell exosomes in the treatment of allergic rhinitis

Clinical study of stem cell exosome nasal spray in the treatment of allergic rhinitis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079863
Enrollment
Unknown
Registered
2024-01-15
Start date
2024-01-16
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

allergic rhinitis

Interventions

treatment group:Nasal application of exosomes
control group:Nasal spray application placebo

Sponsors

Changzhou Third People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria established in the Guidelines for the Diagnosis and Treatment of Allergic Rhinitis (2015, Tianjin); 2. Age: 18-65 years old; 3. Standardized anti allergic drug treatment (including continuous local glucocorticoids, local and oral antihistamines, nasal irrigation, etc.) is ineffective or ineffective; 4. Voluntarily sign an informed consent form, understand and accept the duration of the study, be able and willing to comply with all requirements, including planned treatment, follow-up, and other research procedures.

Exclusion criteria

Exclusion criteria: 1. Suffering from other diseases of the nasal cavity and sinuses (such as nasal polyps, chronic rhinitis, chronic sinusitis, frame structure deformities, etc.); 2. Pregnancy, diagnosis of autoimmune diseases such as systemic lupus erythematosus, rheumatoid arthritis, etc; 3. Patients with serious systemic diseases, such as tumor, digestive tract ulcer, diabetes, tuberculosis, mental disease, etc; 4. Specific infections such as syphilis, leprosy, and tuberculosis; 5. Subjects who have been using immunosuppressants for a long time; 6. The researchers believe that participants who are not suitable to participate in this clinical study.

Design outcomes

Primary

MeasureTime frame
Serum inflammatory factors;Nasal lavage fluid inflammatory factors;Flow cytometric analysis of lymphocyte clusters;

Secondary

MeasureTime frame
Serum specific IgE;endoscopy;olfactometry;

Countries

China

Contacts

Public ContactXue Jianrong

Changzhou Third People's Hospital

entxjr@163.com+86 139 6129 8604

Outcome results

None listed

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