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NCT07019038: NICHE-AIHA
National Longitudinal Cohort of Hematological Diseases- Autoimmune Hemolytic Anemia
trial testing A combined retrospective and prospective observational follow-up in AIHA - Warm Autoimmune Hemolytic Anemia in 9,999 participants. Currently enrolling.
31 December 2070
Quick facts
| Lead sponsor | Institute of Hematology & Blood Diseases Hospital, China |
|---|---|
| Status | Recruiting now |
| Study type | OBSERVATIONAL |
| Enrollment | 9,999 |
| Start date | 1 January 2001 |
| Primary completion | 31 December 2070 |
| Estimated completion | 31 December 2070 |
| Sites | 1 location across China |
Drugs / interventions tested
- A combined retrospective and prospective observational follow-up
Conditions studied
- AIHA - Warm Autoimmune Hemolytic Anemia — all drugs for AIHA - Warm Autoimmune Hemolytic Anemia →
- AIHA - Cold Autoimmune Hemolytic Anemia — all drugs for AIHA - Cold Autoimmune Hemolytic Anemia →
- Autoimmune Hemolytic Anemia Mixed Type — all drugs for Autoimmune Hemolytic Anemia Mixed Type →
Sponsor
Institute of Hematology & Blood Diseases Hospital, China
Who can join
Eligibility, any sex, with AIHA - Warm Autoimmune Hemolytic Anemia or AIHA - Cold Autoimmune Hemolytic Anemia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07019038
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07019038 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Institute of Hematology & Blood Diseases Hospital, China
- Last refreshed: 17 June 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07019038.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing