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Sickle Cell Disease clinical trials

View clinical trials related to Sickle Cell Disease.

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NCT ID: NCT05470270 Completed - Sickle Cell Disease Clinical Trials

Acceptability of a New Paediatric Formulation of Hydroxycarbamide in Children With Sickle Cell Disease.

Start date: July 8, 2022
Phase: Phase 2
Study type: Interventional

This is a prospective, interventional, phase II, open-label, multicentre, national, non-comparative study of a single administration of the new dispersible form of hydroxycarbamide at the usual dose in children with sickle cell disease who are already treated with the current form of hydroxycarbamide (Siklos® 100 mg and/or 1000 mg film-coated tablets).

NCT ID: NCT05392101 Completed - Sickle Cell Disease Clinical Trials

Low Dose Iron Chelation as TReatment of Oxidative Damage in Sickle Cell Disease

TROS
Start date: July 20, 2021
Phase: Phase 2
Study type: Interventional

Objective: To study the safety and efficacy of deferasirox as treatment of oxidative stress in adult subjects with sickle cell disease. Endpoints: The investigators will determine whether treatment with iron chelators results in decreased sickling of RBCs, oxidative stress, neutrophil activation, inflammation, endothelial activation and hypercoagulability and ultimately reduced disease severity. If the hypothesis is confirmed in this pilot dose-finding study, a larger randomized controlled clinical trial will be initiated. Study design: This will be an open-label pilot study, including 12 patients per dose group with a maximum of 3 dose groups. As the antioxidant capacity of deferasirox might be dose-dependent, the investigators will start with the highest dose of deferasirox (360 mg) deemed adequate for chronic use without causing iron depletion in adult SCD patients. Study population: Adult patients with sickle cell anemia (HbSS) or HbS-β0-thalassemia (HbSβ0-thal) visiting the outpatient-clinic of the Academic Medical Center, Amsterdam will be asked for inclusion in the study.

NCT ID: NCT05389891 Completed - Sickle Cell Disease Clinical Trials

Hemoglobinopathy Nursing Program and Pediatric Nursing Students

Start date: February 27, 2017
Phase: N/A
Study type: Interventional

Hemoglobinopathies are the most common life threatening, monogenic disorders in the world. The most common causes of hemoglobinopathies are sickle cell disease and thalassemia. Aim: This study aimed to evaluate the effect of a hemoglobinopathy nursing program on pediatric nursing students' performance.

NCT ID: NCT05371184 Completed - Sickle Cell Disease Clinical Trials

Glutamine Role in Preventing Vaso-occlusive Crisis Among SCD Patients

Glu_SCD_Egy
Start date: January 4, 2022
Phase: Phase 4
Study type: Interventional

Prospective phase IV interventional open label randomized controlled trial to assess safety and efficacy of glutamine in preventing vaso-occlusive crisis (VOC) episodes in sickle cell pediatrics and adolescents' patients

NCT ID: NCT05255445 Completed - Sickle Cell Disease Clinical Trials

Red Blood Cell - IMProving trAnsfusions for Chronically Transfused Recipients

RBC-IMPACT
Start date: March 16, 2022
Phase:
Study type: Observational

Red Blood Cell - IMProving trAnsfusions for Chronically Transfused recipients (RBC-IMPACT) is an observational cohort study to assess donor, component, and recipient factors that contribute to RBC efficacy in chronically and episodically transfused patients. The objective of the study is to determine how specific genetic and non-genetic factors in donors and recipients may impact RBC survival after transfusion - in short, what factors on both the donor and recipient side may improve the efficacy of the transfusion.

NCT ID: NCT05203991 Completed - Sickle Cell Disease Clinical Trials

Avascular Bone Necrosis in Sickle Cell Disease: a Pediatric Study.

OsteoSCD
Start date: March 18, 2021
Phase:
Study type: Observational [Patient Registry]

Avascular necrosis (AVN) is a serious complication of sickle cell disease, especially in pediatric patients where the prevalence is between 3% and 8% and are more frequent in patients with multiple vaso-occlusive crisis (VOC). The prevalence of AVN is usually made by a study of the hip through radiography, whereas other possible sites of ischemic infarcts are evaluated only in case of specific symptoms. In addition, bone infarcts may be the trigger for additional VOC. In this study, we want to investigate the presence of possible bone lesions even in asymptomatic or paucisymptomatic children. This is a prospective interventional and monocentric study whose objective is to describe the prevalence of osteonecrosis in children with sickle cell disease in Italy

NCT ID: NCT05139992 Completed - COVID-19 Clinical Trials

COVID-19 Vaccine Response in Sickle Cell Disease

Start date: December 1, 2021
Phase:
Study type: Observational

The purpose of this study is to assess the antibody response to COVID-19 vaccination in a cohort of patients with sickle cell disease (SCD) and to assess vaccine and SCD related complications around the time of vaccination.

NCT ID: NCT05098028 Completed - Sickle Cell Disease Clinical Trials

Pharmacokinetics and Pharmacodynamics of Rifaximin Novel Formulations in Patients With Sickle Cell Disease

Start date: March 22, 2022
Phase: Phase 2
Study type: Interventional

This is a randomized, double-blind, placebo-controlled study in sickle cell disease participants with a history of Vaso-occlusive Crises (VOCs). Approximately 60 participants with sickle cell disease will be enrolled and randomized: 12 participants in each of four active novel formulation rifaximin groups and 6 participants in each of 2 placebo groups.

NCT ID: NCT05081349 Completed - Sickle Cell Disease Clinical Trials

Hydoxycarbamide and L-Carnitine Therapy in Sickle Cell Anemia

Start date: January 10, 2017
Phase: Phase 4
Study type: Interventional

The role of the combination therapy of hydroxyurea and L-Carnitine was studied in thalassemic patients. nevertheless its role in sickle cell anemia patients was not investigated

NCT ID: NCT05036512 Completed - Sickle Cell Disease Clinical Trials

A Study to Evaluate GBT021601 in Single and Multiple Doses in Healthy Participants

Start date: December 9, 2020
Phase: Phase 1
Study type: Interventional

This first in human study is designed to evaluate the safety, tolerability, pharmacokinetics (PK), and food effect of GBT021601, a hemoglobin S (HbS) polymerization inhibitor, in healthy participants.