Skip to content

Mechanistic Study on the Involvement of lncRNA NEAT1 in the Pathological Process of Allergic Rhinitis via the miR-142-5p/CDK5 Regulatory Axis

Mechanistic Study on the Involvement of lncRNA NEAT1 in the Pathological Process of Allergic Rhinitis via the miR-142-5p/CDK5 Regulatory Axis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104401
Enrollment
Unknown
Registered
2025-06-17
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Allergic rhinitis

Interventions

AR children group :NA
Healthy control group:NA

Sponsors

Huzhou Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 17 Years

Inclusion criteria

Inclusion criteria: Children in the AR group: 1.Meeting the above-mentioned diagnostic criteria for allergic rhinitis (AR); 2.Enrolled children aged between 5 and 17 years old; 3.No history of asthma attacks or other allergic diseases within 6 months prior to enrollment; 4.Immediate family members (or legal guardians) of the participants have provided consent, signed the informed consent form, and the participants voluntarily agree to participate in the study. Healthy control children: 1. Good mental condition, no history of allergic diseases and family history; 2. Age 7~17 years old; 3. Those who can cooperate with the completion of the study.

Exclusion criteria

Exclusion criteria: Children in the AR group: 1.Diagnosed with other allergic diseases requiring long-term medication that cannot be discontinued simultaneously; 2.Presence of deviated nasal septum, or concurrent sinusitis, nasal cavity masses, or other nasal mucosal lesions detected by nasal endoscopy; 3.Suspected or confirmed history of drug abuse; 4.Currently participating in other clinical studies or deemed unsuitable for participation by the investigator; 5.Complicated by other severe primary diseases such as cardiovascular and cerebrovascular diseases, hepatic, renal, or hematopoietic system diseases, autoimmune diseases, congenital genetic metabolic diseases, or psychiatric disorders; 6.Children with AR currently receiving specific immunotherapy; 7.Children whose family members or legal guardians disagree or are unable to cooperate. Healthy control children: 1. Previous history of AR or family history of AR; 2. Those who have poor compliance and are unable to cooperate with the completion of the study; 3. Those who are participating in other clinical studies or are considered inappropriate by the investigator to participate.

Design outcomes

Primary

MeasureTime frame
Expression of lncRNA-NEAT1;Expression of miR-142-5p;Expression of CDK5;

Countries

China

Contacts

Public ContactYang Lihong

Huzhou Center Hospital

huier1982416@163.com+86 572 2555570

Outcome results

None listed

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