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TerminatedNCT00265902Updated Mar 20, 2019

Infrared Thermography in Finding Skin Lesions in Patients With Kaposi's Sarcoma

An interventional study of diagnostic imaging in Sarcoma, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins. Terminated at 1 site in United States. Open to participants aged 18 Years to 120 Years. Per ClinicalTrials.gov, last updated 2019-03-20.

Sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins · Not applicable, Interventional, and Diagnostic

Why this study was terminated
low accrual
Phase
Not applicable
Study type
Interventional
Enrollment
3
Ages
18 Years to 120 Years
Sex
All
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Study summary

RATIONALE: Diagnostic procedures, such as infrared thermography, may help find Kaposi's sarcoma and learn the extent of disease.

PURPOSE: This clinical trial is studying how well infrared thermography finds skin lesions in patients with Kaposi's sarcoma.

Read the detailed description

OBJECTIVES:

Primary

  • Compare ultra-sensitive infrared thermographic images with visible light digital photographic images and clinical dermatologic examination as methods of measuring cutaneous lesions in patients with Kaposi's sarcoma (KS).

Secondary

  • Compare differences in modulation of temperature detected in KS skin lesions with non-involved skin of the same patient and with normal skin of healthy volunteers by sequential imaging using the infrared thermographic camera.

OUTLINE: This is a controlled, pilot study.

Patients undergo clinical assessment followed by simultaneous digital photographic camera imaging and high-resolution infrared thermographic camera imaging of designated normal skin areas and selected marker lesions. Before imaging, a metal bar chilled to 0º C, 10º C, and 25º C is applied to the lesions and designated normal skin areas for up to 90 seconds.

Healthy volunteers (controls) undergo the same procedure as for the patient except only designated normal skin areas are used.

PROJECTED ACCRUAL: A total of 20 patients and 10 healthy volunteers (controls) will be accrued for this study.

02

Conditions studied

  • Sarcoma

Keywords

  • Kaposi sarcoma
03

In context

Sarcoma, Kaposi

162 studies on the registry are indexed under Sarcoma, Kaposi; 29 are open to participants now.

This study's enrollment of 3 is below the median of 32 across 114 interventional studies indexed under Sarcoma, Kaposi.

Browse Sarcoma, Kaposi studies →

Lead sponsor

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins is the lead sponsor of 572 studies on the registry; 73 are open to participants now.

Of its 111 completed or terminated interventional studies of FDA-regulated products, 67 (60%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 120 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

DISEASE CHARACTERISTICS:

  • Meets 1 of the following criteria:

    • Histologically confirmed cutaneous Kaposi's sarcoma (KS)

      • At least one skin lesion accessible for imaging
      • HIV positivity with proven cutaneous KS and concurrent visceral or mucous membrane involvement allowed
    • Healthy volunteer (regardless of HIV status) (control)

PATIENT CHARACTERISTICS:

Performance status

  • Not specified

Life expectancy

  • Not specified

Hematopoietic

  • Not specified

Hepatic

  • Not specified

Renal

  • Not specified

Other

  • Pregnancy allowed

PRIOR CONCURRENT THERAPY:

  • Prior topical, intralesional, or systemic treatment allowed
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Enrollment
3 participants (actual)

Interventions

  • Procedurediagnostic imaging
06

Study locations

1 site
  • Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
    Baltimore, Maryland 21231-2410, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 20, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00265902
Lead sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Collaborators
National Cancer Institute (NCI)
Responsible party
Sponsor
First posted
Dec 15, 2005
Start date
Oct 3, 2005
Primary completion
Mar 21, 2006
Completion
Mar 21, 2006
Last update
Mar 20, 2019

Study contacts

Ciro Martins, MD
study chair · Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jun 2006. You cannot join it, but the record below documents what was studied.

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