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RECRUITING Not applicable ClinicalTrials.gov

Precision Imaging to Evaluate Kaposi Sarcoma

Sponsor: Washington University School of Medicine • ClinicalTrials.gov ID: NCT06898203

Registry updated: 2026-09-21
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Description

AIMS 2 \& 3: In this study the investigators seek to formally compare reproducibility and accuracy of KS lesion size measurements between SkinScan3D and the current standard of care manual measurement method. The investigators will then test the SS3D device on 100 patients in a variety of real-world practice locations to determine whether the device will be usable, acceptable, appropriate, and feasible in routine care settings.

Interventions

  • SkinScan3D (Device)
    A handheld, simple, low-cost, and user-friendly technology that combines liquid lens technology and artificial intelligence (AI).

Eligibility criteria

Inclusion Criteria - Aim 2 (Patients): * Adults age ≥18 years old * Histopathology-confirmed Kaposi Sarcoma * At least 3 skin lesions * Capable of informed consent * On treatment for Kaposi Sarcoma Exclusion Criteria - Aim 2 (Patients): * Patients not initiating Kaposi Sarcoma treatment * Very ill patients requiring hospitalization Inclusion Criteria - Aim 3 (Patients): * Adults age ≥18 years old * Histopathology-confirmed Kaposi Sarcoma * Capable of informed consent * Initiating treatment for Kaposi Sarcoma Exclusion Criteria - Aim 3 (Patients): * Patients with Kaposi Sarcoma that participated in Aim 1 or Aim 2 * Prior or ongoing Kaposi Sarcoma treatment

Conditions

Kaposi Sarcoma

Locations

  • Kenya Medical Research Institute — Kisumu, Kenya
  • Infectious Diseases Institute, Makerere University — Kampala, Uganda
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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record