Clinical Trials Directory

Trials / Terminated

TerminatedNCT05111821

Iron Chelation in the Prevention of Secondary Degeneration After Stroke

Long-term Iron Chelation in the Prevention of Secondary Remote Degeneration After Stroke

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
11 (actual)
Sponsor
University Hospital, Bordeaux · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Stroke is a major cause of disability over the world. While acute therapies have made huge progresses, the number of survivors leaving with clinical consequences of stroke is increasing. Beyond stroke itself, secondary neurodegeneration of disconnected areas, especially of central hubs such as the substantia nigra or the thalamus, could significantly impact the overall outcome of the patients. Data have identified iron accumulation within the disconnected areas as potentially accelerating neurodegeneration. In this research, the main objective is test whether long-term chelation through Deferiprone (Ferrirpox®, Chiesi) administered daily from 3-to-5 days following stroke to 6 months could avoid iron accumulation as measured with Magnetic resonance imaging (MRI) within disconnected areas (substantia nigra). MRI imaging methods such as the quantification of the transverse relaxation rate R2\* provide highly correlated information to the histologically measured iron load

Conditions

Interventions

TypeNameDescription
PROCEDUREMagnetic Resonance Imaging (MRI)Quantification of iron will be performed through Magnetic Resonance Imaging
DRUGDeferiprone treatmentPatients receiving Deferiprone during 6 months. Oral deferiprone for 6 months at a dose of 30 mg/kg/d

Timeline

Start date
2022-06-08
Primary completion
2025-04-17
Completion
2025-04-22
First posted
2021-11-08
Last updated
2025-07-21

Locations

2 sites across 1 country: France

Source: ClinicalTrials.gov record NCT05111821. Inclusion in this directory is not an endorsement.