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Evaluating the Accuracy of Microvessel Ultrasound Imaging for Detecting Extent of Disease in Patients With Angiosarcoma of the Skin

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Mayo Clinic

Status

Terminated

Conditions

Skin Angiosarcoma

Treatments

Device: Ultrasound Microvessel Imaging

Study type

Observational

Funder types

Other

Identifiers

NCT05729425
NCI-2022-09609 (Registry Identifier)
21-005183 (Other Identifier)

Details and patient eligibility

About

This study evaluates the accuracy of a new ultrasound technology called microvessel imaging for detecting the extent of disease among patients with angiosarcoma of the skin. Microvessel ultrasound imaging uses high frequency waves to visualize vessels in the skin that are not easily seen using other imaging tests.

Full description

PRIMARY OBJECTIVE:

I. To determine the accuracy of depicting extent of disease of cutaneous angiosarcoma before and after neoadjuvant treatment compared to clinical photographs, magnetic resonance imaging (MR) or positron emission tomography (PET)/computed tomography (CT) imaging and surgical pathology both on skin biopsies and surgical excision.

OUTLINE:

Patients undergo microvessel ultrasound imaging on study.

Enrollment

1 patient

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Diagnosed with cutaneous angiosarcoma of the breast or scalp and scheduled for trimodality therapy
  • Twenty one years of age or older

Exclusion criteria

  • Unwilling to consent to microvessel ultrasound imaging
  • Younger than 21 years of age

Trial design

1 participants in 1 patient group

Observational (microvessel ultrasound imaging)
Description:
Patients undergo microvessel ultrasound imaging on study.
Treatment:
Device: Ultrasound Microvessel Imaging

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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