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Genetic Testing in Detection of Late-Onset Hearing Loss (SoundGene)

28. februar 2012 opdateret af: Pediatrix

Utility of Genetic Testing in Detection of Late-Onset Hearing Loss

Two major limitations of existing audiometric newborn hearing screening programs are their inability to detect forms of deafness that are not expressed at birth and the low compliance with obtaining recommended audiologic confirmation and/or follow-up. Molecular genetic tests on blood spots from all newborns will identify those at risk for the most frequent causes of late-onset hearing loss and to add these infants to the group who should receive continued audiologic monitoring.

Studieoversigt

Status

Afsluttet

Intervention / Behandling

Detaljeret beskrivelse

Two major limitations of existing audiometric newborn hearing screening programs are their inability to detect forms of deafness that are not expressed at birth and the low compliance with obtaining recommended audiologic confirmation and/or follow-up. Molecular genetic tests on blood spots from all newborns will identify those at risk for the most frequent causes of late-onset hearing loss and to add these infants to the group who should receive continued audiologic monitoring.

The specific aims of this project are to:

  • Demonstrate the utility of detecting four potentially important causes of delayed onset hearing loss by molecular tests at birth, which may be missed by current audiometric screening tests.
  • Document the frequency, clinical and genetic characteristics of hearing loss associated with each condition.

Dried blood spots (DBS) on filter paper will be obtained and be used for this project with parental informed consent from 6,000 newborn infants at approximately 25 hospitals. Pediatrix Screening, a subsidiary of Pediatrix Medical Group with long experience in high throughput neonatal testing, will perform genetic testing on the samples. The four genetic and environmental forms of deafness to be studied include:

  • Prenatal/congenital cytomegalovirus (CMV) infection

    -Detecting the presence of CMV viral DNA in dried blood spots.

  • Connexin Deafness - GJB2 and GJB6 mutations

    - Cx26 35delG, Cx26 235delC, Cx26 167delT, Cx26 M34T, and Cx30 large deletion.(Under sublicense with Athena Diagnostics, Inc: United States Patent Numbers: 5,998,147 and 6,485,908 and patents pending)

  • Pendred Syndrome - SLC26A mutations

    - L236P, 1001 +1G>A, T416P, E384G

  • Mitochondrial Mutations - T961C, T961G, G951A, 961 delT+C(n)Ins, G7444A, A7445G, A7445C.

Undersøgelsestype

Observationel

Tilmelding (Faktiske)

3681

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Kansas
      • Topeka, Kansas, Forenede Stater, 66604
        • Stormont-Vail HealthCare
    • Ohio
      • Dayton, Ohio, Forenede Stater, 45409
        • Miami Valley Hospital
    • Oklahoma
      • Oklahoma City, Oklahoma, Forenede Stater, 73112
        • Integris Baptist Medical Center

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

Ikke ældre end 2 uger (Barn)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

Hospital

Beskrivelse

Inclusion Criteria:

  • Documentation of informed consent
  • Inborn
  • Ability to do ABR (auditory brainstem response screen technology) screening test on all participants
  • Age at enrollment less than 14 days or less than or equal to 336 hours (Birth date is day 0)
  • Gestational age > = 34 0/7 weeks and above. (Late preterm infants and term infants)
  • No major anomalies
  • Ability to obtain blood sample prior to administration of any blood product transfusion
  • Subjects' parents or legal guardian willing to provide follow-up data on their child. They will need to provide a telephone contact number and address for follow-up procedures

Exclusion Criteria:

  • Older than 14 days of age or 336 hours
  • Receipt of a blood product prior to the ability to obtain blood sample for genetic testing (SoundGene panel)
  • Any major congenital anomalies. (chromosomal abnormalities, cyanotic congenital heart disease, gastroschisis, omphalocele, diaphragmatic hernia, or other major gastrointestinal anomalies, major neurological injury or anomaly, and multiple congenital anomalies)

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Efterforskere

  • Ledende efterforsker: Gail Lim, ARNP, Pediatrix
  • Studiestol: Zhili Lin, MD, PhD, Pediatrix Screening
  • Studiestol: Reese H Clark, MD, Pediatrix

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. oktober 2007

Primær færdiggørelse (Faktiske)

1. september 2009

Studieafslutning (Faktiske)

1. september 2011

Datoer for studieregistrering

Først indsendt

2. august 2007

Først indsendt, der opfyldte QC-kriterier

2. august 2007

Først opslået (Skøn)

3. august 2007

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

1. marts 2012

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

28. februar 2012

Sidst verificeret

1. februar 2012

Mere information

Begreber relateret til denne undersøgelse

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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