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Thrombocytopenia clinical trials

View clinical trials related to Thrombocytopenia.

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NCT ID: NCT04915482 Recruiting - Clinical trials for Connective Tissue Diseases

TPO-RAs Combined With Anti-CD20 Antibody in the Treatment of Adult Immune Thrombocytopenia With Autoantibodies

Start date: June 6, 2021
Phase: Phase 2/Phase 3
Study type: Interventional

This prospective, open-label, nonrandomized, multicenter clinical trial aims at comparing the efficacy and safety of combined use of TPO-RAs with low-dose anti-CD20 monoclonal antibody vs. the best available therapy(BAT)in adult immune thrombocytopenia with autoantibodies failed (due to intolerance or resistance) to first-line treatment.

NCT ID: NCT04915287 Recruiting - Clinical trials for Chronic Liver Disease

Efficacy of Avatrombopag in Thrombocytopenic Patients With Chronic Liver Disease Undergoing an Elective Procedure

Start date: June 6, 2021
Phase: Phase 4
Study type: Interventional

In this study, investigators aimed to evaluate the efficacy of Avatrombopag in thrombocytopenic patients with chronic liver disease undergoing an elective invasive procedure through a prospective, non-randomized controlled, multicenter clinical trial. The patients were non-randomly assigned to the Avatrombopag group (119 patients) and the conventional treatment group (357 patients). The primary endpoint was the proportion of patients not requiring prophylactic platelet transfusion or rescue therapy due to bleeding from grouping up to 10 days post-procedure. Second endpoints included the proportion of patients achieving a platelet count of ≥50x10^9/L and the mean change in platelet count from baseline at the time before the procedure, the proportion of patients requiring platelet transfusion and the mean platelet transfusion units per capita, the incidence of bleeding events (WHO≥2 and requiring rescue therapy), the imaging evaluations of bleeding events, the incidence of adverse events, the changes in life quality between two groups before and after treatment, and the pharmacoeconomic index of two groups. Note: According to the results of interim statistical analysis (200-300 cases), it is up to the sponsor to decide whether to terminate the study in advance or increase the number of included cases at a later stage.

NCT ID: NCT04912505 Recruiting - Clinical trials for Purpura, Thrombocytopenic

ASPirin in Immune thRombocytopenia Patients With Cardiovascular disEase

ASPIRE
Start date: January 16, 2023
Phase: Phase 2
Study type: Interventional

The incidence of immune thrombocytopenia increases with older age. This population is at risk for arterial thrombosis. Due to an increased turn-over of platelets, low-dose aspirin once daily may be insufficient in this population to protect against arterial thrombosis. This study is aimed at assessing the pharmacodynamics of aspirin once daily on platelet function in these patients.

NCT ID: NCT04906083 Recruiting - Thrombocytopenia Clinical Trials

Avatrombopag in Patients With End-stage Liver Disease and Thrombocytopenia

Start date: February 1, 2021
Phase: Phase 4
Study type: Interventional

End stage liver disease is prone to thrombocytopenia. This study is a multi-center, randomized, prospective, randomized controlled Phase IV Clinical trial to discuss the Efficacy and Safety of Avatrombopag in Patients with End-stage Liver Disease and Thrombocytopenia.

NCT ID: NCT04904276 Terminated - Clinical trials for Immune Thrombocytopenia

Observational Study of Fostamatinib as Second Line Therapy in Adult Patients With Immune Thrombocytopenia (ITP) and Insufficient Response to a Prior Therapy

Start date: May 18, 2021
Phase:
Study type: Observational

Evaluate patient characteristics, treatment patterns, clinical outcomes and safety of fostamatinib as second-line therapy in real-world clinical practice, for the treatment of ITP in adult patients who have an insufficient response to prior therapy (steroids ± immunoglobulins).

NCT ID: NCT04902807 Not yet recruiting - Clinical trials for Systemic Lupus Erythematosus

Conception of a Diagnosis, Prognosis and Therapeutic Decision Tool for Patients With Autoimmunity and Inflammation

ATRACTion
Start date: June 2021
Phase:
Study type: Observational

The main objective of this study is to generate diagnosis and therapeutic-decision tools through the identification of molecular causes of PIDs with autoimmunity/inflammation and the variability in disease outcome at the transcriptional level using a combination of omics signatures (transcriptomics, epigenomics, proteomics, metagenomics, metabolomics and lipidomics).

NCT ID: NCT04896528 Recruiting - Thrombocytopenia Clinical Trials

Efficacy and Safety of Avatrombopag in Cancer Patients With Thrombocytopenia

Start date: June 6, 2021
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy and safety of Avatrombopag in patients with thrombocytopenia induced by targeted therapy and immunotherapy combination treatment, and provide evidence-based medication for the clinical use of Avatrombopag in patients with PC ≤50×109/L

NCT ID: NCT04890041 Recruiting - Clinical trials for Primary Immune Thrombocytopenic Purpura

TPO-RA in Primary Immune Thrombocytopenia (ITP) in Patients Older Than 14 Years

ITP
Start date: May 30, 2021
Phase: N/A
Study type: Interventional

This multi-center study aims to study the efficacy of TPO-RAs' transformation in Chinese ITP patients older than 14 years. This study will be conducted in ITP patients who had not responded to first-line in the previous treatment .

NCT ID: NCT04889326 Recruiting - Covid19 Clinical Trials

Collection of the Thrombo-VaxCov Cohort

THROMBO-VAXCOV
Start date: April 2, 2021
Phase:
Study type: Observational

In the context of anti-Covid19 vaccination, atypical thrombosis have occured and potential link with vaccination is under investigation. This study collect clinical and biological data of all atypical thrombosis occurring within 4 weeks after antiCovid vaccination.

NCT ID: NCT04873102 Recruiting - Cirrhosis, Liver Clinical Trials

Danazol for Treatment of Cytopenias in Patients With Cirrhosis

Start date: May 2023
Phase: Phase 2
Study type: Interventional

This is a phase II pilot study designed to assess the safety and efficacy of danazol for treatment of cytopenias in patients with CPC A/B cirrhosis. Subjects with or without telomere mutations and/or shortened telomeres will be treated with danazol 600 mg per day by mouth for a duration of 24 months. The goal will be to treat a total of 10 patients.