Far Infrared Radiation Treatment for Prostate Cancer
Phase 1 Study to Evaluate the Efficacy of Using Energy Specific Far Infrared Radiation Treatment for Prostate Cancer
1 other identifier
interventional
4
1 country
1
Brief Summary
A study to determine the use of far infrared radiation for the treatment of prostate cancer.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_1
Started Jan 2006
Typical duration for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2006
CompletedFirst Submitted
Initial submission to the registry
December 12, 2007
CompletedFirst Posted
Study publicly available on registry
December 14, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2008
CompletedAugust 17, 2009
August 1, 2009
2.1 years
December 12, 2007
August 14, 2009
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The primary end point is to determine the therapeutic effects of far infrared radiation on Prostate Cancer.
2 years and 6 months
Secondary Outcomes (1)
The secondary end point of the study is to evaluate the therapeutic effects of far infrared radiation on other types of cancer (Bladder and Testis).
2 years and 6 months
Study Arms (1)
1
OTHERInterventions
Far Infrared Radiation (5μm to 20μm wavelength) for 30 to 40 minutes each treatment session.
Eligibility Criteria
You may qualify if:
- Persons with Prostate, Bladder or Testicular Cancer.
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Centre for Incurable Diseases
Toronto, Ontario, M4V 1L5, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ken Nedd, M.D.
GAAD Medical Research Institute Inc.
- STUDY DIRECTOR
Kwasi Donyina, Ph.D.
GAAD Medical Research Institute Inc.
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
December 12, 2007
First Posted
December 14, 2007
Study Start
January 1, 2006
Primary Completion
February 1, 2008
Study Completion
December 1, 2008
Last Updated
August 17, 2009
Record last verified: 2009-08