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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT02776995
Date of registration: 10/05/2016
Prospective Registration: No
Primary sponsor: Sheba Medical Center
Public title: Tumor Monitoring Using Thermography During Radiation Therapy
Scientific title: Tumor Monitoring Using Thermography During Radiation Therapy
Date of first enrolment: November 2014
Target sample size: 80
Recruitment status: Recruiting
URL:  https://clinicaltrials.gov/show/NCT02776995
Study type:  Interventional
Study design:  Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Other. Masking: None (Open Label).  
Phase:  N/A
Countries of recruitment
Israel
Contacts
Name:     Merav Ben-David, MD
Address: 
Telephone: 972-3-5305086
Email: merav.ben-david@sheba.health.gov.il
Affiliation: 
Name:     Merav Ben-David, MD
Address: 
Telephone:
Email:
Affiliation:  Sheba Medical Center
Key inclusion & exclusion criteria

Inclusion Criteria:

- signed informed consent

- will undergo radiation therapy for palliation or curative intent due to cancer, biopsy
proven

Exclusion Criteria:

- not eligible to sign informed consent



Age minimum: 18 Years
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Malignancy
Intervention(s)
Other: Thermography imaging
Primary Outcome(s)
Measurement of IR : Infra-Red radiation emitted at wavelengths 0.8-1nm [Time Frame: Before the first fraction of radiation and every 5 fraction until the end of radiation therapy, approximately 4-5 weeks.]
Secondary Outcome(s)
Dermal side effects during radiation therapy using CTCAE v4.0 [Time Frame: Before the first fraction of radiation and every 5 fraction until the end of radiation therapy, approximately 4-5 weeks.]
US/CT scans [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.]
Secondary ID(s)
1216-14-SMC
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Tel Aviv University
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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