Darbepoetin for Ischemic Neonatal Stroke to Augment Regeneration

Who is this study for? Infant patients with Perinatal Arterial Ischemic Stroke
What treatments are being studied? Darbepoetin Alpha
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The aim of the study is to perform a randomized double-blind placebo controlled prospective study in newborn infants with MRI confirmed Middle Cerebral Artery (MCA) Perinatal Arterial Ischemic Stroke (PAIS) with darbepoetin. It will be investigated whether intravenous administered darbepoetin can induce the formation of neuronal tissue and restore brain function in neonates who suffered from PAIS compared to placebo treated controls. The ultimate goal of this study is therefore to develop a therapy using erythropoiesis-stimulating agents (ESA) such as darbepoetin to reduce or even prevent lifelong consequences of PAIS-related brain injury in this group of term newborns.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 7 days
Healthy Volunteers: f
View:

• Newborns ≥ 36+0 weeks of gestation, both male and female

• MRI confirmed diagnosis of acute PAIS, in the MCA region with involvement of the cortical spinal tract (e.g. Posterior Limb of Internal Capsule \[PLIC\] or peduncles) within one week after birth

• Written informed consent from custodial parent(s)

Locations
Other Locations
Netherlands
Wilhelmina Childrens Hostpital/University Medical Center Utrecht
RECRUITING
Utrecht
Contact Information
Primary
Manon Benders, MD PhD
m.benders@umcutrecht.nl
+31 88 755 5555
Backup
Lisanne M Baak, MD
l.m.baak-3@umcutrecht.nl
+31 88 755 5555
Time Frame
Start Date: 2017-07-01
Estimated Completion Date: 2025-06-01
Participants
Target number of participants: 80
Treatments
Experimental: Darbepoetin
Darbepoetin alfa (Aranesp, Amgen)
Placebo_comparator: Placebo
Saline
Related Therapeutic Areas
Sponsors
Collaborators: Alberta Children's Hospital, The Hospital for Sick Children
Leads: UMC Utrecht

This content was sourced from clinicaltrials.gov

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