Evidence map›Paper›PMID 34439518›Full record

ArticleAntioxidants (Basel, Switzerland)2021

Targeting Pro-Oxidant Iron with Deferoxamine as a Treatment for Ischemic Stroke: Safety and Optimal Dose Selection in a Randomized Clinical Trial.

Mònica Millán, Núria DeGregorio-Rocasolano, Natàlia Pérez de la Ossa, Sílvia Reverté, Joan Costa, Pilar Giner, Yolanda Silva, Tomás Sobrino, Manuel Rodríguez-Yáñez, Florentino Nombela and 7 more

Registry-linked trialAbstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00777140 (Double-blind, Randomized, Placebo Controlled, Dose-finding Phase 2 Clinical Trial of Intravenous Deferoxamine in Patients With Acute Ischemic Stroke Treated With Tissue Plasminogen Activator), which is not on this map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00777140 phase2completednot on this map

Double-blind, Randomized, Placebo Controlled, Dose-finding Phase 2 Clinical Trial of Intravenous Deferoxamine in Patients With Acute Ischemic Stroke Treated With Tissue Plasminogen Activator

TypeinterventionalSponsorGermans Trias i Pujol HospitalRan2008 to 2011Enrolled62ConditionsIschemic Stroke, AcuteArmsDeferoxamine
3 · Its place in the literature

Who cites it

45 citing papers in PubMed.

  1. Ferroptosis in heatstroke: Mechanisms and therapeutic perspectives (Review).International journal of molecular medicine · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Mònica MillánDepartment of Neurosciences, Hospital Germans Trias i Pujol, 08916 Badalona, Barcelona, Spain.
Núria DeGregorio-RocasolanoDepartment of Neurosciences, Hospital Germans Trias i Pujol, 08916 Badalona, Barcelona, Spain.ORCID 0000-0001-5248-7525
Natàlia Pérez de la OssaDepartment of Neurosciences, Hospital Germans Trias i Pujol, 08916 Badalona, Barcelona, Spain.
Sílvia RevertéDepartment of Neurosciences, Hospital Germans Trias i Pujol, 08916 Badalona, Barcelona, Spain.ORCID 0000-0002-2052-9978
Joan CostaDepartment of Clinical Pharmacology, Hospital Germans Trias i Pujol, 08916 Badalona, Barcelona, Spain.
Pilar GinerDepartment of Pharmacy, Hospital Germans Trias i Pujol, 08916 Badalona, Barcelona, Spain.
Yolanda SilvaDepartment of Neurology, Hospital Dr. Josep Trueta, 17007 Girona, Spain.
Tomás SobrinoClinical Neurosciences Research Laboratory, Health Research Institute of Santiago de Compostela, Hospital Clínico Universitario, Universidade de Santiago de Compostela, 15706 Santiago de Compostela, Spain.ORCID 0000-0002-9760-8690
Manuel Rodríguez-YáñezDepartment of Neurology, Hospital Clínico Universitario, 15706 Santiago de Compostela, Spain.
Florentino NombelaDepartment of Neurology, Hospital La Princesa, 28006 Madrid, Spain.
Francisco CamposClinical Neurosciences Research Laboratory, Health Research Institute of Santiago de Compostela, Hospital Clínico Universitario, Universidade de Santiago de Compostela, 15706 Santiago de Compostela, Spain.ORCID 0000-0001-8665-1039
Joaquín SerenaDepartment of Neurology, Hospital Dr. Josep Trueta, 17007 Girona, Spain.
José VivancosDepartment of Neurology, Hospital La Princesa, 28006 Madrid, Spain.
Octavi Martí-SistacCellular and Molecular Neurobiology Research Group, Department of Neurosciences, Germans Trias i Pujol Research Institute (IGTP), 08916 Badalona, Barcelona, Spain.
Jordi CortésDepartment of Statistics and Operations Research, Universitat Politècnica de Catalunya (UPC), 08028 Barcelona, Spain.ORCID 0000-0002-3764-0795
Antoni DávalosDepartment of Neurosciences, Hospital Germans Trias i Pujol, 08916 Badalona, Barcelona, Spain.ORCID 0000-0003-2949-5679
Teresa GasullDepartment of Neurosciences, Hospital Germans Trias i Pujol, 08916 Badalona, Barcelona, Spain.ORCID 0000-0002-9321-1741

Funding

Agència de Gestió d'Ajust Universitaris i de Recerca 2019PROD00120Agència de Gestió d'Ajuts Universitaris i de Recerca 2017 SGR 1520Instituto de Salud Carlos III 2007-006731-31Instituto de Salud Carlos III RD16/0019/0020
6 · The paper itself

Abstract

A role of iron as a target to prevent stroke-induced neurodegeneration has been recently revisited due to new evidence showing that ferroptosis inhibitors are protective in experimental ischemic stroke and might be therapeutic in other neurodegenerative brain pathologies. Ferroptosis is a new form of programmed cell death attributed to an overwhelming lipidic peroxidation due to excessive free iron and reactive oxygen species (ROS). This study aims to evaluate the safety and tolerability and to explore the therapeutic efficacy of the iron chelator and antioxidant deferoxamine mesylate (DFO) in ischemic stroke patients. Administration of placebo or a single DFO bolus followed by a 72 h continuous infusion of three escalating doses was initiated during the tPA infusion, and the impact on blood transferrin iron was determined. Primary endpoint was safety and tolerability, and secondary endpoint was good clinical outcome (clinicalTrials.gov NCT00777140). DFO was found safe as adverse effects were not different between placebo and DFO arms. DFO (40-60 mg/Kg/day) reduced the iron saturation of blood transferrin. A trend to efficacy was observed in patients with moderate-severe ischemic stroke (NIHSS > 7) treated with DFO 40-60 mg/Kg/day. A good outcome was observed at day 90 in 31% of placebo vs. 50-58% of the 40-60 mg/Kg/day DFO-treated patients.

Indexed as

antioxidantdeferoxamineferroptosisironneuroprotectionoutcome

Identifiers

PMID34439518
PMCPMC8389327

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.