Construction of a Database for TMA

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorThe First Affiliated Hospital of Soochow University

About this trial

Information about patients was collected by reviewing the Hitech case system and telephone and outpatient follow-up, and the case database was constructed by Epidata software. The sample size is expected to be 200 cases, the participating hospital is the First Affiliated Hospital of Soochow University, and the study time frame is from Dec 1, 2022, to Nov 31, 2027. The observation indexes of the study include the basic information of patients' age and gender and the clinical-related data of thrombotic microangiopathy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

The investigator considers the subject unable or unwilling to cooperate with the study procedures.

Trial population

A total of 500 eligible TMA patients are to be collected for this project.

Trial design

Design model

Case-only

Time perspective

Cross-sectional

Treatments tested in this trial

  • collection data

    Other intervention

    collection data

Treatment groups

500 Participants
are divided into 1 treatment group
Group A: TMA1 intervention

Trial outcomes

Primary outcomes

1

Number of participants with stroke

Stroke was assessed with MRI imaging.

Time frame
5 years from the time of entering the database.

Secondary outcomes

Other outcomes

Sponsors and contacts

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