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Thrombocytopenia clinical trials

View clinical trials related to Thrombocytopenia.

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NCT ID: NCT05983952 Recruiting - Thrombocytopenia Clinical Trials

Anti-CD38 Antibody Treating APS With Thrombocytopenia

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

To evaluate the safety and efficacy of anti-CD38 antibody in the treatment of antiphospholipid syndrome with secondary thrombocytopenia in patients who have not responded adequately or relapsed after first-line treatment and at least one second-line therapy including rituximab and/or TPO-RA.

NCT ID: NCT05980806 Recruiting - Myelofibrosis Clinical Trials

A Study of Selinexor Monotherapy in Subjects With JAK Inhibitor-naïve Myelofibrosis and Moderate Thrombocytopenia

SENTRY-2
Start date: April 22, 2024
Phase: Phase 2
Study type: Interventional

The main purpose of this study with corresponding optional expansion is to evaluate the efficacy of selinexor in JAKi-naïve participants with myelofibrosis (MF) and moderate thrombocytopenia based on spleen volume reduction (SVR). Additional efficacy and safety parameters will also be assessed during the study.

NCT ID: NCT05969158 Not yet recruiting - Clinical trials for Chemotherapy-Induced Thrombocytopenia

Hetrombopag in Secondary Prevention of XPO-1 Inhibitor-induced Thrombocytopenia in Lymphoma

Start date: September 4, 2023
Phase: Phase 2
Study type: Interventional

To explore the efficacy and safety of hetrombopag for secondary prevention of thrombocytopenia caused by XPO-1 inhibitor Selinexor combined with chemotherapy in patients with lymphoma.

NCT ID: NCT05958511 Not yet recruiting - Thrombocytopenia Clinical Trials

Assessment of Risk Factors and Outcome of Thrombocytopenia in ICU Patients

Start date: September 1, 2023
Phase:
Study type: Observational

The many comorbidities in the severely ill patient also make thrombocytopenia very common (∼ 40%) in intensive care unit patients. The risk of bleeding is high with severe thrombocytopenia and is enhanced in intensive care patients with mild or moderately low platelet counts when additional factors are present that interfere with normal hemostatic mechanisms (eg, platelet function defects, hyperfibrinolysis, invasive procedures, or catheters).

NCT ID: NCT05944809 Recruiting - Esophageal Cancer Clinical Trials

The Effect of Prophylactic TPO Combined With BMS-IMRT to Esophageal Cancer Patients

Start date: July 20, 2023
Phase: Phase 2
Study type: Interventional

The goal of this interventional study is to explore the protective effect of prophylactic TPO combined with bone marrow sparing (BMS)-IMRT in patients with esophageal cancer undergoing concurrent chemoradiotherapy. The main purpose is to reduce the incidence of all grades of thrombocytopenia from 35% to less than 10% by the intervention of study. Participants will initiate concurrent chemoradiotherapy within 2 weeks after enrollment,and they will receive subcutaneous injection of recombinant human thrombopoietin (rhTPO) 15000U once a week during the radiotherapy.

NCT ID: NCT05944458 Recruiting - Clinical trials for Linezolid Induced Thrombocytopenia

The Effect of NAC in Decreasing the Incidence of Linezolid-induced Thrombocytopenia in Critically Ill Patients

Start date: August 1, 2023
Phase: Phase 4
Study type: Interventional

- Study the effect of acetylcysteine on decreasing the incidence of LIT in critically ill patients. - Study the impact of acetylcysteine on the time to onset of LIT and the time to recovery of platelets.

NCT ID: NCT05944445 Recruiting - Clinical trials for Thrombocytopenia; Drugs

The Incidence of Linezolid-induced Thrombocytopenia (LIT) in Critically Ill Patients, the Risk Factors for LIT

Start date: July 13, 2023
Phase:
Study type: Observational

- To identify the incidence of LIT among critically ill patients, as limited studies have only addressed this population. - To evaluate the impact of several factors on the incidence of LIT, the time to onset of LIT, and the time to recovery of platelets. - To study the effect of concurrent medications (enoxaparin, unfractinated heparin, piperacillin, carbapenems, tigecycline, fluconazole or voriconazole, digoxin, amiodarone, acetaminophen, tirofiban, statins, and antiepileptics) frequently used in critically ill patients on the incidence of LIT. - To investigate the impact of possible medications with an antioxidant effect on the prevention of LIT. - To assess the impact of LIT on composite end point (mortality, bleeding, and length of stay)

NCT ID: NCT05944211 Not yet recruiting - Clinical trials for Chemotherapy-Induced Thrombocytopenia

Hetrombopag for the Treatment of Chemotherapy-Induced Thrombocytopenia(CIT) in Patients With Acute Myeloid Leukemia

H-CIT-AML
Start date: July 2023
Phase: Phase 2
Study type: Interventional

Randomized, controlled, open study to evaluate the efficacy and safety of Hetrombopag in the treatment of chemotherapy-induced thrombocytopenia(CIT) in patients with acute myeloid leukemia

NCT ID: NCT05943691 Recruiting - Clinical trials for ITP - Immune Thrombocytopenia

High-dose Dexamethasone Plus Hetrombopag vs High-dose Dexamethasone Alone as Frontline Treatment for Newly Diagnosed Adult Primary Immune Thrombocytopenia: A Prospective, Multicenter, Randomized Trial

Start date: September 15, 2023
Phase: Phase 2
Study type: Interventional

The project was undertaking by Qilu Hospital of Shandong University in China. In order to report the efficacy and safety of Hetrombopag plus high-dose dexamethasone for the treatment of adults with newly-diagnosed primary immune thrombocytopenia (ITP).

NCT ID: NCT05937828 Recruiting - Clinical trials for Immune Thrombocytopenia

OBS'CEREVANCE: French Cohort of Pediatric Autoimmune Cytopenia

OBS'CEREVANCE
Start date: September 1, 2010
Phase:
Study type: Observational [Patient Registry]

From 2004, OBS'CEREVANCE is a national real-world prospective clinical cohort of patients with auto-immune cytopenia of pediatric-onset : Immune thrombocytopenia (ITP), Autoimmune Hemolytic anemia (AIHA), or Evans syndrome (all bi or tri cytopenias). Thanks to the collaboration of the 30 French pediatric hematologic centers, this cohort supports all of the Rare Disease Centre CEREVANCE (Centre de Référence National des Cytopénies Auto-Immunes de l'Enfant) missions for care, education and research. Specifically, this original unbiased database allows to describe the long-term health of adult patients, to identify the heterogenous genetic underlying pathophysiologic contexts, and to study the benefit-risk balance of treatments, including the growing development of targeted therapies.