Clinical Trials Logo

Clinical Trial Summary

A prospective cohort study of thrombotic thrombocytopenic purpura and atypical hemolytic uremic syndrome patients who have presented with their acute episode and are in remission within the last 30 days. They will be followed for 12 months from the time of their initial scan, followed by a long-term follow up study.


Clinical Trial Description

The investigators will conduct a prospective cohort study at the London Health Sciences Centre, Ontario, Canada. The investigators will identify 15-30 idiopathic thrombotic thrombocytopenic purpura and atypical hemolytic uremic syndrome patients who are in remission within the last 30 days. They will be followed for 12 months from the time of their remission. Study procedures include routine laboratory monitoring, biomarker assessments, cardiovascular and neurocognitive functional assessments, and non-invasive imaging studies. The long-term follow-up thrombotic thrombocytopenic purpura and atypical hemolytic uremic syndrome study will help to assess the mechanisms of vascular injuries, evaluate cardiovascular and cerebrovascular monitoring tools, and generate novel ideas to prevent further vascular injuries. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03187652
Study type Observational
Source Lawson Health Research Institute
Contact Huang
Phone 519-685-8500
Email shuang45@uwo.ca
Status Recruiting
Phase
Start date January 1, 2017
Completion date January 1, 2026

See also
  Status Clinical Trial Phase
Recruiting NCT03605511 - TTP and aHUS in Complicated Pregnancies
Recruiting NCT05785468 - A Retrospective, Observational Study on the Response to Caplacizumab Treatment in aTTP Patients: the Italian Experience (ROSCAPLI)
Completed NCT04074187 - A Trial of Caplacizumab in Japanese Patients With Acquired Thrombotic Thrombocytopenic Purpura (aTTP) Phase 2/Phase 3
Terminated NCT00953771 - Safety Study of Danazol With Plasma Exchange and Steroids for the Treatment of Thrombotic Thrombocytopenic Purpura (TTP) Phase 2
Recruiting NCT01257269 - Genotype and Phenotype Correlation in Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman Syndrome)
Not yet recruiting NCT05568147 - Aspirin for Prophylaxis of TTP Phase 2/Phase 3
Recruiting NCT05468320 - Caplacizumab and Immunosuppressive Therapy Without Firstline Therapeutic Plasma Exchange in Adults With Immune-mediated Thrombotic Thrombocytopenic Purpura Phase 3
Completed NCT00713193 - Study of Cyclosporine or Corticosteroids as an Adjunct to Plasma Exchange in Thrombotic Thrombocytopenic Purpura (TTP) Phase 3
Completed NCT00426686 - ADAMTS13 in Thrombotic Thrombocytopenic Purpura N/A
Withdrawn NCT00251277 - Use of Rituximab Treatment in Addition to Standard Care for Newly Presenting Thrombotic Thrombocytopenic Purpura Phase 1/Phase 2
Recruiting NCT04588194 - Romiplostim, Rituximab and Dexamethasone as Frontline Treatment for Immune Thrombocytopenia Phase 2
Active, not recruiting NCT03237819 - Magnesium Sulfate in Thrombotic Thrombocytopenic Purpura in Intensive Care Phase 3
Completed NCT00907751 - Rituximab in Adult Acquired Idiopathic Thrombotic Thrombocytopenic Purpura Phase 2
Completed NCT03369314 - Observational Study of the Use of octaplasLG®.
Terminated NCT01938404 - Octaplas Adult TTP Trial
Recruiting NCT04981028 - The ConNeCT Study: Neurological Complications of TTP
Completed NCT02134171 - Early Predictive Factors of Cardiac and Cerebral Involvement in TMA N/A
Recruiting NCT05389007 - .German TTP-Registry (Thrombotic Thrombocytopenic Purpura)
Withdrawn NCT02626663 - The Role of Microparticles as a Biomarker
Completed NCT01931644 - At-Home Research Study for Patients With Autoimmune, Inflammatory, Genetic, Hematological, Infectious, Neurological, CNS, Oncological, Respiratory, Metabolic Conditions