Actively Recruiting
Construction of a Database for Thrombotic Microangiopathy
Led by The First Affiliated Hospital of Soochow University · Updated on 2022-12-02
500
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are collecting detailed information on patients with thrombotic microangiopathies (TMA) to build a comprehensive database. This observational study is conducted by the First Affiliated Hospital of Soochow University and aims to gather clinical data, including basic demographics like age and gender, as well as disease-related measurements. The study is planned to include around 200 patients and runs from December 1, 2022, to November 30, 2027. The study involves reviewing patient information through the Hitech case system, telephone follow-ups, and outpatient visits. Data is compiled and managed using Epidata software to construct the database. Participants are patients diagnosed with TMA who meet specific clinical criteria related to blood markers and pathological findings. There is no intervention or treatment being administered; rather, the focus is on data collection and observation. Participants will be followed over time, with researchers monitoring key outcomes such as the occurrence of stroke within five years of entering the database. The study collects clinical data and demographic information through medical records and follow-ups. This monitoring helps researchers understand the progression and complications associated with TMA, with the overall participation lasting up to five years after enrollment.
CONDITIONS
Brief Title
Construction of a Database for TMA
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
- More than 2% of schistocytes visible on a peripheral blood smear
- Alternatively, pathological sections show extensive micro thrombosis
You will not qualify if you...
- The investigator considers the subject unable or unwilling to cooperate with the study procedures
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 5 years
Participants with thrombotic microangiopathy are observed over time to collect clinical data.
Visits as per routine clinical care
Trial Site Locations
Total: 1 location
1
The First Affiliated Hospital of Soochow University
Suzhou, Jiangsu, China, 215006
Actively Recruiting
Research Team
Y
Yue Han, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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