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Iron Overload clinical trials

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NCT ID: NCT06468423 Completed - Clinical trials for Pateints of ß-thalassemia Major With Iron Overload

Comparison of Deferasirox and Desferoxamine in Patients of β-Thalassemia Major With Iron Overload

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

This study was planned to compare deferasirox and desferrioxamine in terms of mean serum ferritin levels in patients of β-thalassemia major having Iron overload. Choosing an effective iron chelator is crucial to increasing iron chelation therapy compliance. Not much local data exists in Pakistan comparing the effectiveness of deferasirox (DFX) and desferrioxamine (DFO), so, this study would be helpful in providing baseline data and formulating new protocols for iron chelation therapy, in which DFX may be a useful oral alternative to parenteral DFO.

NCT ID: NCT06421636 Not yet recruiting - Clinical trials for Non-transfusion Dependent Beta-thalassemia (NTDT)

A Study to Test the Safety, Tolerability, and Efficacy of an Antibody, REGN7999, Injected Under the Skin for the Treatment of Iron Overload in Adult Participants With Non-Transfusion Dependent β-thalassemia, Using MRI Scans to Measure Iron Levels in the Body

FERVENT-1
Start date: September 25, 2024
Phase: Phase 2
Study type: Interventional

This study is researching an experimental drug called REGN7999 (called "study drug"). The study is focused on patients with non-transfusion dependent beta-thalassemia. The aim of the study is to see how safe and effective the study drug is. The study is looking at several other research questions, including: - Whether the study drug lowers extra iron levels in the body - What side effects may happen from taking the study drug - How much study drug is in the blood at different times - Whether the body makes antibodies against the study drug (which could make the drug less effective or could lead to side effects)

NCT ID: NCT06215287 Completed - Clinical trials for Chronic Iron Overload

Survey to Assess Physicians' Knowledge of Exjade Posology and Biological Monitoring Recommendations as Described in the Educational Materials

Start date: January 12, 2024
Phase:
Study type: Observational

The objective of this survey is to assess the knowledge of HCPs in relation to the recommended posology and biological monitoring for Exjade, based on the current locally valid Exjade educational materials (including the physician's reference checklist)

NCT ID: NCT06146608 Recruiting - Iron Overload Clinical Trials

Heme and Non-heme Iron Intakes, Gut Microbiota, and Influence on Host Iron Absorption

FeMicrobiome
Start date: January 15, 2023
Phase:
Study type: Observational

The FeMicrobiome study will evaluate gut microbiome features and their relationships with dietary iron absorption in healthy adults. The investigators hypothesize that (1) the gut microbiota can be shaped by the heme and non-heme Fe content of the diet and that (2) this will influence individual variation in dietary Fe absorption.

NCT ID: NCT06137079 Recruiting - Iron Overload Clinical Trials

"Iron Overload and Endocrinological Diseases"

Start date: June 20, 2013
Phase:
Study type: Observational

Patients with hemochromatosis or Thalassemia develop progressive tissue and organs damages secondary to iron overload. Iron overload can result both from transfusional hemosiderosis and excess gastrointestinal iron absorption. Iron deposition in the heart, liver, and multiple endocrine glands results in severe damage to these organs, with variable degrees of endocrine and organ failure. Although patients with iron overload often present endocrine disorders, the pathogenetic mechanisms underlying endocrinopathies are not completely clear. In particular it is not elucidated if the spectrum of endocrinopathies could change with advancing age. All endocrinological comorbidities can develop from a primary damage of the target gland, from pituitary secondary failure or from both. The aim of this study is to investigate the prevalence of endocrinological diseases in adult patients with iron overload due to β-thalassemia or hemochromatosis and their impact on well-being and quality of life. The study design is a prospective cross-sectional clinical study. All subjects enrolled will be evaluated for the endocrine diseases. The study protocol will include data collection from family and patients' history of diseases, physical examination, hormonal assessment for all endocrine axes and instrumental examinations. The results will provide evidence on the prevalence of endocrine diseases in patients with iron overload and will add information to characterize the type and the degree of endocrine deficiencies, and on the pathogenic mechanisms involved, in order to individualize diagnostic and therapeutic approaches.

NCT ID: NCT05777733 Not yet recruiting - Thalassemia Major Clinical Trials

NAC Effect on Iron Overload and Blood Transfusion in β-thalassemia Major

Start date: March 23, 2024
Phase: Phase 1
Study type: Interventional

The effect of N_acetylcystein as an antioxidant on iron overload and frequency of blood transfusion in β-thalassemia major patients at Assiut Childern Hospital University And its cosubmitted for partial fulfillment of master degree in Pediatrics

NCT ID: NCT05586932 Not yet recruiting - Clinical trials for Oxidative Stress in Patient With Haemoglobinopathy and Affect it of Endocrine System

Oxidative Stress and Iron Overload in Patient With Abnormal Haemoglobinopathy

Start date: December 1, 2022
Phase:
Study type: Observational

The effects of iron overload and oxidative stress and dyslipidemia on glucose level and thyroid function in patients with abnormal hemoglobinopathy. 2- Evaluation of MDA level as a marker of oxidative stress.

NCT ID: NCT05440487 Completed - Clinical trials for Chronic Iron Overload

Study to Assess Iron Chelation Therapy in Patients With Chronic Iron Overload

EXCALIBUR
Start date: September 15, 2015
Phase:
Study type: Observational

This is a prospective, multicenter, non-interventional study. Findings are analyzed using epidemiological methods.

NCT ID: NCT05355766 Recruiting - Thalassemia Clinical Trials

Long-term Clinical Study of CN128 in Thalassemia With Sever Liver Iron Overloaded Patients

Start date: June 2, 2022
Phase: Phase 2
Study type: Interventional

The safety and efficacy of CN128 is studied in thalassaemia with sever liver iron overloaded patients.

NCT ID: NCT05326503 Not yet recruiting - Thalassemia Clinical Trials

Inhibitory Effect of a Polyphenol Supplement on Dietary Iron Absorption in Adults With Thalassemia

Start date: May 1, 2022
Phase: N/A
Study type: Interventional

Genetic disorders, such as thalassemia, can lead to iron overload and severe adverse health outcomes. In iron-loading thalassemia, iron overload is due to increased iron absorption. Iron accumulates in the body organs causing widespread damage. The standard treatment is iron chelation therapy and/or periodic phlebotomy to remove iron from the body; frequency of phlebotomy or chelation therapy is dependent on how quickly body iron stores accumulate. Polyphenolic compounds are very strong inhibitors of non-heme iron absorption, as they form insoluble complexes with ferrous iron in the gastrointestinal tract that cannot be absorbed. The investigators have recently shown in European subjects with hereditary hemochromatosis (another iron-loading disorder) that our newly-developed natural polyphenol supplement (PPS) that is rich in polyphenols, when taken with iron-rich meals or with an iron-fortified drink, reduces iron absorption by ~40%. Decreasing non-heme iron absorption in adults with iron-loading thalassemia could potentially lead to an extension of the time period between phlebotomies or chelation therapies, and therefore an improved quality of life. Therefore, in this stable iron isotope study, the investigators will study the effect the natural PPS on oral iron absorption from an iron-rich test meal or iron-fortified drink in Thai adults with iron-loading thalassemia.