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Completed • Phasen NA • Stufe 0, I, II, III, IV • Post-Menopausal • Interventionell

Folgendes wird aus ClinicalTrials.gov importiert:

Accuracy of FNA Versus CNB of Abnormal Axillary Lymph Nodes in Setting of Invasive Breast Cancer

To compare accuracy of ultrasound guided fine needle aspiration (FNA) to core needle biopsy (CNB) of ultrasound detected abnormal axillary lymph nodes in patients with newly diagnosed invasive breast cancer or suspected invasive breast cancer. Hypothesis: FNA and CNB have equivalent diagnostic accuracies In order to prove our hypothesis, we will perform FNA and CNB on the same lymph node in each consented patient. The two samples will be evaluated separately by different pathologists blinded to the material in the other sample. The results of the biopsies will be compared to the gold standard (lymph node excision).

Breast Cancer

Studiendesign
Studientyp:

Interventional

Geschätzte Einschreibung:

140 Teilnehmer

Aktueller Studienbeginn:

20. Februar 2014

Zulassungskriterien
Alter für die Studie berechtigt:

18 - 999

Geschlechter für die Studie berechtigt:

both


Arms and Intervention
  • FNA and Core biopsy

Einschlusskriterien
  • recent or suspected diagnosis of invasive breast cancer with abnormal ipsilateral axillary lymph node

  • able to provide informed consent

Ausschlusskriterien
  • lymph node not amenable to core biopsy

  • patient is unlikely to undergo lymph node excision (i.e. elderly patient with co-morbidities)

Trial Information at Site
Last Updated:
Studieninformationen
ClinicalTrial.gov ID:

Completed

Estimated Enrollment:

140

Last Updated:

11/03/2022


Studiensponsor

University of Utah

Study Location (2)

Huntsman Cancer Hospital

Salt Lake City, Utah, United States

Huntsman Cancer Hospital

Salt Lake City, Utah, United States

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