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Evaluation of diagnostic efficacy of total IgE antibody detection kit (colloidal gold method)

Evaluation of total IgE antibody detection kit (colloidal gold method) for the diagnosis of allergic conjunctivitis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100051949
Enrollment
Unknown
Registered
2021-10-09
Start date
2021-11-01
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Allergic conjunctivitis

Interventions

Gold Standard:Itching symptoms, accompanied by conjunctival congestion, conjunctival papilla, corneal specific lesions at least one of the three signs.
Detection&#32
Kit&#32

Sponsors

Xiangyang First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who suspected or highly suspected clinical symptoms or confirmed allergic conjunctivitis.

Exclusion criteria

Exclusion criteria: Patients with other eye diseases.

Design outcomes

Primary

MeasureTime frame
Total IgE concentration in the tear;

Countries

China

Contacts

Public ContactQian Zhuyun

Beijing GiantMed Diagnostics Laboratory Co. LTD

qianzhuyun552@126.com+86 13817109809

Outcome results

None listed

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