Creating a database for patients with thrombotic microangiopathies
Official title: Construction of a Database for Thrombotic Microangiopathy
Run by The First Affiliated Hospital of Soochow University · NCT05634928 · Data updated 2026-11-12
This study is creating a detailed database to collect important information about patients with thrombotic microangiopathies to help improve understanding and treatment of the condition.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | The First Affiliated Hospital of Soochow University Academic / other |
| Locations | 1 site (Suzhou, Jiangsu) |
| Status | Recruiting |
| Started | December 1, 2022 |
| Main results expected | November 30, 2027 |
| Study ends | November 30, 2028 |
| Registry record updated | December 2, 2022 |
| Trial ID | NCT05634928 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients exhibiting specific laboratory criteria indicative of thrombotic microangiopathies.
✕Probably not a fit
Patients who are unable or unwilling to cooperate with the study procedures will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to construct a comprehensive database for patients diagnosed with thrombotic microangiopathies by collecting detailed clinical data. Patient information will be gathered through the Hitech case system and follow-up via telephone and outpatient visits. The study will include approximately 200 cases and will take place at the First Affiliated Hospital of Soochow University from December 2022 to November 2027, focusing on key clinical indicators such as age, gender, and specific laboratory findings related to the condition.
Why it matters
Potential benefit: If successful, this database could enhance understanding and management of thrombotic microangiopathies, leading to improved patient outcomes.
How similar studies have gone: While this approach is observational and data-driven, similar studies have successfully utilized patient databases to improve understanding of complex conditions.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * The patient has elevated lactate dehydrogenase to more than twice the baseline value, platelets less than 20 or decreased by more than 50% within 24 hours, and more than 2% of schistocytes visible on a peripheral blood smear. Alternatively, pathological sections show extensive micro thrombosis. Exclusion Criteria: * The investigator considers the subject unable or unwilling to cooperate with the study procedures.
Where it's running
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The First Affiliated Hospital of Soochow University
Suzhou, Jiangsu, China Recruiting
Study contacts
- Study coordinator: Yue Han, PhD
- Email: hanyue@suda.edu.cn
- Phone: +86 18913091817
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.