← Eichor
Study identifier: NCT05950750 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Turkey Thrombotic Thrombocytopenic Purpura Disease Registry: National Multicenter Study

Condition: TTP - Thrombotic Thrombocytopenic Purpura  ·  Sponsor: Turkish Hematology Association

PhaseN/A
Planned participants960
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

21 hematology centers in Turkey will participate in this noninterventional observational study. The recruitment target is 960 cases. Patients will be followed-up at least 1 year or to the end of the study according to the physicians' discretion, or withdrawal of consent. Recruitment period will be 36 months. Data will be collected via electronic case report form. Since the study cohort does not include only newly diagnosed patients, all aTTP patients will be included to the study, previous treatments and diagnosis information data could also be collected from hospital records. Patients recruitment duration: 3 years (36 months) Patients follow-up duration: 1 year (12 months)

This description comes directly from the study's public registry record.

Talk to the study team

ilker kurkcu  ·  +905326354515  ·  ilker.kurkcu@sentez-cro.com

Always discuss trial participation with your own doctor first.

Locations (1)

Baskent Universtiy Faculty of MedicineAnkara, Turkey (Türkiye)Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05950750