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National Longitudinal Cohort of Hematological Diseases- Autoimmune Hemolytic Anemia (NICHE-AIHA)

I

Institute of Hematology & Blood Diseases Hospital, China

Status

Enrolling

Conditions

AIHA - Warm Autoimmune Hemolytic Anemia
AIHA - Cold Autoimmune Hemolytic Anemia
Autoimmune Hemolytic Anemia Mixed Type

Treatments

Other: A combined retrospective and prospective observational follow-up

Study type

Observational

Funder types

Other

Identifiers

NCT07019038
NICHE-AIHA

Details and patient eligibility

About

Hematological diseases are disorders of the blood and hematopoietic organs. The current hematological cohorts are mostly based on single-center or multi-center cases, or cohorts with limited sample size in China. There is a lack of comprehensive and large-scale prospective cohort studies in hematology.

The objectives of this study are to investigate the incidence and risk factors of autoimmune hemolytic anemia (AIHA) and to analyze the treatment effectiveness, patient prognosis and healthcare costs in China.

  1. Analyze the demographic and clinical characteristics of patients with AIHA, including sex, age, disease severity, and other relevant factors.
  2. Examine disease features of AIHA patients, such as biochemical and hematological indicators
  3. Assess treatment patterns and real-world effectiveness in AIHA patients.
  4. Evaluate clinical outcomes, including hematologic response, relapse, and mortality
  5. Investigate long-term prognosis, including post-discontinuation outcomes and health-related quality of life.

Enrollment

9,999 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects diagnosed with AIHA.
  • Hemoglobin<100g/L
  • Subjects treated at the Institute of Hematology and Blood Diseases Hospital from Jan 1, 2001.

Exclusion criteria

  • Subject unlikely to be available for long-term follow-up for any reason (e.g., inability to obtain follow-up data or presence of severe comorbidities).
  • Subject with alcohol or drug dependence may reduce their compliance with the study.
  • Subjects that the investigator believes have other reasons that make them unsuitable for inclusion in this study.

Trial design

9,999 participants in 1 patient group

NICHE-AIHA
Description:
Patients who were diagnosed with AIHA in the investigating hospitals from Jan 1, 2001.
Treatment:
Other: A combined retrospective and prospective observational follow-up

Trial contacts and locations

1

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Central trial contact

Lele Zhang, PhD

Data sourced from clinicaltrials.gov

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