CClinicalTrials.gg
Status unknownNCT02776995Updated Apr 9, 2019

Tumor Monitoring Using Thermography During Radiation Therapy

An interventional study of Thermography imaging in Malignancy, sponsored by Sheba Medical Center. Status unknown at 1 site in Israel. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-04-09.

Sponsored by Sheba Medical Center · Not applicable, Interventional, and Other

The sponsor has not verified this record recently (last verified Apr 2019), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Not applicable
Ages
18 Years and older
Sex
All
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Study summary

This research aims to investigate the correlation between tumor temperature difference and biological factors, such as size, metabolism, treatment response, and tumor aggressiveness.

In addition, normal tissue response to adjuvant radiation therapy in treated organs following surgery, will be evaluated.

Read the detailed description

During radiation session, the investigators would evaluate the changes that will be detected by thermal imaging and correlate them with visible side effects as well as with known tumor biology factors and skin-tumor distance.

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Conditions studied

  • Malignancy

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03

In context

Neoplasms

9,365 studies on the registry are indexed under Neoplasms; 2,486 are open to participants now.

This study's planned enrollment of 80 is above the median of 50 across 7,250 interventional studies indexed under Neoplasms.

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Lead sponsor

Sheba Medical Center is the lead sponsor of 660 studies on the registry; 63 are open to participants now.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • signed informed consent
  • will undergo radiation therapy for palliation or curative intent due to cancer, biopsy proven

Exclusion criteria

Exclusion Criteria:

  • not eligible to sign informed consent
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Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
80 participants (estimated)

Study arms

  • Other
    Patients undergoing radiation

    In this study, patients undergoing radiation treatment will undergo thermography imaging during radiation treatment course. Patients will be evaluated with thermography imaging every 5 fraction of radiation, starting prior to the first radiation treatment, periodically, until the end of radiation therapy (a period of several weeks).

    Other: Thermography imaging

Interventions

  • OtherThermography imaging

    Thermography imaging of the treated - irradiated body area.

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What researchers measure

Primary outcomes

  1. Measurement of IR : Infra-Red radiation emitted at wavelengths 0.8-1nm

    Mathematical analysis of the thermic image

    Time frame: Before the first fraction of radiation and every 5 fraction until the end of radiation therapy, approximately 4-5 weeks.

Secondary outcomes

  1. Dermal side effects during radiation therapy using CTCAE v4.0

    Clinical assesment of the side effects by physician.

    Time frame: Before the first fraction of radiation and every 5 fraction until the end of radiation therapy, approximately 4-5 weeks.

  2. US/CT scans

    The tumor size will be measures to evaluate the efficacy of the radiation treatment.

    Time frame: The tumor size in cubic cm will be mesured prior to first fraction of radiation, and 2 weeks following the end of radiation session. Time for final evaluation: approximately 6-7 weeks.

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Study locations

1 of 1 sites recruiting
  • Merav Ben David
    Ramat-Gan, Israel
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 9, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02776995
Lead sponsor
Sheba Medical Center
Collaborators
Tel Aviv University
Responsible party
Dr. Merav Ben-David (Medical and Radiation Oncologist, Head of Breast Radioation Unit, Sheba Medical Center) — Principal investigator
First posted
May 19, 2016
Start date
Nov 2014
Primary completion
Dec 30, 2020 (estimated)
Completion
Dec 30, 2020 (estimated)
Last update
Apr 9, 2019

Study contacts

Merav Ben-David, MD
Contact
merav.ben-david@sheba.health.gov.il
972-3-5305086
Zvi Symon, MD
Contact
zvi.symon@sheba.health.gov.il
972-3-5305080
Merav Ben-David, MD
principal investigator · Sheba Medical Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2019. You cannot join it, but the record below documents what was studied.

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