Actively Recruiting

All Genders
ID05634928

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

All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

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

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

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

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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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