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Search / Trial NCT06751355

Precision Imaging to Evaluate Kaposi Sarcoma (PRIME-KS): A Device Feasibility Trial

Launched by WASHINGTON UNIVERSITY SCHOOL OF MEDICINE · Dec 20, 2024

Trial Information

Current as of July 26, 2025

Recruiting

Keywords

Kaposi Imaging Photography 3 D

ClinConnect Summary

The PRIME-KS trial is studying a new way to take detailed 3D images of Kaposi sarcoma (KS), a type of cancer that can occur in people with HIV/AIDS. This trial aims to improve how doctors assess the size and shape of KS lesions, which are the growths caused by this cancer. The new imaging system, called SkinScan3D, uses advanced technology to capture more accurate information than traditional 2D images, helping to better monitor how well treatments are working over time.

To participate in this trial, you need to be at least 18 years old and have been diagnosed with Kaposi sarcoma, with at least three visible lesions on your skin. If you join, you can expect to have your KS lesions photographed using this innovative imaging technology. This could help researchers understand how KS responds to different treatments and may lead to better care for patients in the future. The trial is currently recruiting participants, so if you meet the criteria and are interested, you may want to learn more about it.

Gender

ALL

Eligibility criteria

  • Eligibility Criteria:
  • Have been diagnosed with histologically or cytologically proven Kaposi sarcoma (KS).
  • Has at least 3 cutaneous Kaposi sarcoma lesions.
  • At least 18 years of age.
  • Ability to understand and willingness to sign an IRB approved written informed consent document.

About Washington University School Of Medicine

Washington University School of Medicine is a leading academic medical institution renowned for its commitment to advancing healthcare through innovative research, education, and patient care. With a strong emphasis on translating scientific discoveries into practical applications, the institution conducts a diverse array of clinical trials aimed at improving treatment outcomes and enhancing the understanding of various medical conditions. Its collaborative environment fosters partnerships between researchers, clinicians, and community stakeholders, ensuring that the trials not only contribute to scientific knowledge but also address the pressing health needs of diverse populations.

Locations

Saint Louis, Missouri, United States

Patients applied

0 patients applied

Trial Officials

Lee Ratner, M.D., Ph.D.

Principal Investigator

Washington University School of Medicine

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported