- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02386228
Micro Ribonucleic Acid (miRNA) Markers of Hydrocephalus in Intraventricular Hemorrhage (IVH)
5. januar 2017 oppdatert av: Madelon Petersen, St. Joseph's Hospital and Medical Center, Phoenix
miRNA Markers of Hydrocephalus in Intraventricular Hemorrhage (IVH)
A collection of biological samples (cerebrospinal fluid [CSF] and blood) from patients under 6 years of age who are diagnosed with intraventricular hemorrhage or spina bifida.
Studieoversikt
Status
Avsluttet
Intervensjon / Behandling
Detaljert beskrivelse
IVH is an important cause of brain injury in newborns and more so in those born prematurely.
Depending on the severity of the hemorrhage and the care provided the newborn, the impact of IVH can range from a temporary issue with no permanent consequences to a life-threatening condition with severe neurodevelopmental sequelae.
The outcomes of patients with IVH are not only dictated by the direct effects of the hemorrhage, but to associated processes such as hydrocephalus, periventricular infarction and leukomalacia.
Despite the availability of better diagnostic and therapeutic tools, the incidence of IVH has remained constant over the past 50 years, and is mostly due to the increased survival rates of very low weight premature infants.
Recent statistics demonstrate that close to 12,000 premature infants develop IVH in the United 'states every year and more than 50% of them develop some degree of posthemorrhagic hydrocephalus (PHH).
It is believed that PHH originates as a result or arachnoiditis, gliosis, and subsequent fibrosis impairing the flow and reabsorption of cerebrospinal fluid (CSF).
Despite the lack of clarity about the pathogenesis of PHH, it is well accepted that its presence exacerbates the damage caused by the hemorrhage to the periventricular white matter.
Multiple efforts have been made to identify the mechanisms and mediators of the development of PHH and white matter damage.
Molecules such as transforming growth factor-beta (TGF-beta) have been demonstrated to enhance the expression of genes encoding for fibronectin, collagen and other extracellular matrix components.
Unfortunately, not enough evidence has been generated to be able to envision a potential solution for the problem.
The current management of PHH is focused on controlling the damage that pressure, distortion, and/or ischemia may cause to the immature brain.
Direct evacuation of ventricular contents with CSF diversion mechanisms remains, such as sequential lumber punctures, external ventricular draining, and reservoir placement.
Intraventricular fibrinolytic therapy or permanent shunting represent most effective tools by mechanically evacuating bleeding products and preventing the accumulation of CSF.
However, they are all highly invasive techniques that carry major risks and complications.
The use of diuretics has been presented as a non-invasive alternative, but the results prove them inefficient.
Extracellular miRNA sequences have been found to be major modulators of protein coding genes involved in differentiation, proliferation, and apoptosis.
Several studies have reported the presence of significant amounts of miRNA in extracellular fluids such as plasma, urine, saliva, and semen.
The researchers believe that extracellular miRNAs are present in CSF and that sequential evaluation of their expression can provide a unique biomarker signature, time sensitive enough to reflect the evolution of pathological events underlying the development of PHH.
The identification of a miRNA biomarker for PHH development and/or hemorrhagic related injury would also be a means to quickly evaluate treatment response.
Studietype
Observasjonsmessig
Registrering (Faktiske)
1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Arizona
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Phoenix, Arizona, Forente stater, 85013
- St. Joseph's Hospital and Medical Center
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Ikke eldre enn 6 år (Barn)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Prøvetakingsmetode
Ikke-sannsynlighetsprøve
Studiepopulasjon
infants with IVH or spina bifida
Beskrivelse
Inclusion Criteria:
- Age between 0 and 6 years.
- Diagnosis of IVH or spina bifida
- Granted access to CSF and blood via surgery, CSF diversion device, venous access, and/or arterial access.
Exclusion Criteria:
- Older than 6 years.
- Diagnosis of infection or other acute inflammatory process involving the central nervous system.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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miRNA sequences
Tidsramme: within 30 days of blood or CSF collection
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Identification of miRNA sequences common to patients with IVH and patients with spina bifida to determine condition specific expression profiles, multivariate analysis of candidate miRNA sequences that are differentially expressed between the two conditions but between different outcomes (development of hydrocephalus) to target potential markers.
Once identified, mechanisms for the rapid detection of marker sequences will be developed and their predictive value tested in future collections.
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within 30 days of blood or CSF collection
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Robert Spetzler, MD, Barrow Brain and Spine physician with SJHMC privileges
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. mars 2015
Primær fullføring (Faktiske)
1. desember 2016
Studiet fullført (Faktiske)
1. desember 2016
Datoer for studieregistrering
Først innsendt
5. mars 2015
Først innsendt som oppfylte QC-kriteriene
10. mars 2015
Først lagt ut (Anslag)
11. mars 2015
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
6. januar 2017
Siste oppdatering sendt inn som oppfylte QC-kriteriene
5. januar 2017
Sist bekreftet
1. januar 2017
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
- Patologiske prosesser
- Kardiovaskulære sykdommer
- Vaskulære sykdommer
- Cerebrovaskulære lidelser
- Hjernesykdommer
- Sykdommer i sentralnervesystemet
- Sykdommer i nervesystemet
- Medfødte abnormiteter
- Misdannelser i nervesystemet
- Intrakranielle blødninger
- Nevralrørsdefekter
- Blødning
- Hjerneblødning
- Hydrocephalus
- Spinal dysrafi
Andre studie-ID-numre
- 14BN104
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