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Incidence of genetic abnormalities in patients with primary hypereosinophilia

Incidence of genetic abnormalities in patients with primary hypereosinophilia

Status
Unknown
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20210514006
Enrollment
151
Registered
2021-05-14
Start date
2020-12-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

The patient 18 years and older ,The patients diagnosed with primary hypereosinophilia leukocyte count more than 1,500 per microliter for a period of more than 1 month. Incidence of genetic abnormalities in patients with primary hypereosinophilia.

Interventions

The patient 18 years and older ,The patients diagnosed with primary hypereosinophilia leukocyte count more than 1,500 per microliter for a period of more than 1 month in field of hamatology .
Diagnostic
he patient 18 years and older ,The patients diagnosed with primary hypereosinophilia .

Sponsors

Siriraj Hospital Mahidol University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) The patients diagnosed with primary hypereosinophilia type white blood cells greater than 1,500 per microliter for a period of more than 1 month 2) 18 years of age and over 3) Patients who received the gene test The specific targeted fusion gene panel with hypereosinophilia 4) was welcomed to join the program by signing.

Exclusion criteria

Exclusion criteria: 1.The patient was detected from a bacterial infection by antibody detection Research projects in which patients are examined. Incidence of nasopharyngeal carcinoma in patients primary hypereosinophilias 686 / 2563 (IRB2) 2.Patients with allergic history 3.Asthma patients 4. Patients with immune diseases 5 Patients diagnosed with various cancers are not in peacetime. 6. History of steroid use in patients with herbs or drugs in the past three months 7. The patients had a history of adverse events leading to leukocyte disease, hypertension, and xa0; Penicillin, cephalosporin, GM-CSF, NSAID, ranitidine, isopropanol, isopropanol, alanine, amazillin sulfate, chlorazine, chlorazine Cyclospora

Design outcomes

Primary

MeasureTime frame
Mutations in hypereosinophilic patients first clinic visit Next generation sequencing for targeted gene mutations

Secondary

MeasureTime frame
Overall survival 5 years From medical record (date of diagnosis, date of death, and date of last follow up)

Countries

Thailand

Contacts

Public ContactWeerapat Owattanapanich

Division of Hematology,Faculty of Medicine Siriraj Hospital, Mahidol University .

weerapat36733@gmail.com0891081983

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026