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Digital Breast Tomosynthesis Versus Digital Mammography: A National Multicenter Trial

31. januar 2012 opdateret af: Thomas Moritz, Medical University of Vienna

Digital Breast Tomosynthesis vs. Digital Mammography: A National Multicenter Trial

The goal of this study is to determine the value of the new mammography technique called Digital Breast Tomosynthesis (DBT) compared to the current standard technique Digital Mammography for the early detection of Breast Cancer.

DBT is able to compute a three-dimensional image of a breast from several low-dose mammographies taken from different angles while the device is moving around the breast in a circular motion. This should overcome a significant limitation of Digital Mammography arising from the masking of breast cancer in a mammography image caused by overlying normal breast tissue.

This is a study conducted in several Austrian Breast Imaging Centers.

Studieoversigt

Status

Ukendt

Betingelser

Detaljeret beskrivelse

This prospective national multicenter multivendor trial aims at determining the impact of the novel technique Digital Breast Tomosynthesis (DBT) in the assessment and screening for breast cancer. Mammography is the primary imaging modality for the early detection of clinically occult breast cancer.

Despite advances in mammographic technique, mammography is still limited with regard to both sensitivity and specificity. In the majority of cases these limitations arise from the masking of subtle breast cancer lesions by overlapping breast tissue.

DBT is a novel technique that tries to overcome these limitations by performing a 3D-reconstruction of breast tissue from multiple low-dose digital mammographic images acquired in several planes in a 15 to 50 degree angle.

Early studies indicate an advantage of DBT compared to the standard Full Field Digital Mammography (FFDM) in terms of an improvement of specificity without cutback in sensitivity.

Controversy continues over the use of DBT in combination with FFDM or as a standalone screening method without concomitant 2D imaging. Unfortunately, the peer-reviewed publications evaluating DBT are limited and consist of single institution studies with a small number of participants.

The purpose of this study is to evaluate the novel technique of DBT compared to routine FFDM in a clinical large sample study (600 participants) to provide the path to implementation of this new technique into clinical and screening routine.

Undersøgelsestype

Observationel

Tilmelding (Forventet)

600

Kontakter og lokationer

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

Studiesteder

      • Vienna, Østrig, A-1090
      • Vienna, Østrig, A-1100
      • Vienna, Østrig, A-1140
        • Rekruttering
        • Hanusch Krankenhaus
        • Kontakt:
    • Styria
      • Graz, Styria, Østrig, A-8036
    • Upper Austria
      • Wels, Upper Austria, Østrig, A-4600

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

25 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Kvinde

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

The study population consists of two groups:

One screening group consisting of asymptomatic women (Age 40+) referred for a screening mammography examination.

The second group consists of women aged 25+ referred for further examination of a breast lesion.

Beskrivelse

Inclusion Criteria:

  • Age > 25 years (40 years or older for Screening Cohort)
  • No history of breast cancer
  • Written informed consent
  • Asymptomatic women in follow up for early detection of breast cancer or
  • Patients with a recent positive mammography (BI-RADS 3-5)

Exclusion Criteria:

  • Pregnant and breast feeding women
  • Unable to tolerate breast compression
  • Breast implants
  • Unable to understand or execute written informed consent

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Kohorter og interventioner

Gruppe / kohorte
Breast Cancer Screening Patients
Group 1 consists of Women referred to Breast Cancer Screening examinations at a participating Austrian Breast Imaging Site
Diagnostic Patients
Patients referred to a participating Breast Imaging Center for a clinically or radiologically detected breast lesion

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Specificity of Digital Breast Tomosynthesis in the characterization of Breast lesions
Tidsramme: One year
One year

Sekundære resultatmål

Resultatmål
Tidsramme
Sensitivity of Digital Breast Tomosynthesis in the detection of malignant breast lesions
Tidsramme: One year
One year

Samarbejdspartnere og efterforskere

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

Efterforskere

  • Ledende efterforsker: Thomas Moritz, MD, Medical University of Vienna
  • Studieleder: Thomas Helbich, MD Prof. MBA MSc, Medical University of Vienna

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. januar 2012

Primær færdiggørelse (Forventet)

1. september 2012

Studieafslutning (Forventet)

1. december 2012

Datoer for studieregistrering

Først indsendt

29. januar 2012

Først indsendt, der opfyldte QC-kriterier

31. januar 2012

Først opslået (Skøn)

1. februar 2012

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

1. februar 2012

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

31. januar 2012

Sidst verificeret

1. januar 2012

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • TomoTrial001

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 .

Kliniske forsøg med Brystneoplasmer

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