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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00599482
Other study ID # GAAD-SCC-CTP1
Secondary ID
Status Active, not recruiting
Phase Phase 1
First received January 11, 2008
Last updated January 2, 2009
Start date January 2008
Est. completion date January 2009

Study information

Verified date January 2009
Source GAAD Medical Research Institute Inc.
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

Most patients with sickle-cell disease have periodic intensely painful episodes. To manage this pain, we are proposing the drinking of at least 500 mL of water followed by far infrared radiation.


Description:

Painful sickle cell crises are treated with hydration and analgesics. Ischemia is an absolute or relative shortage of the blood supply to an organ. Relative shortage means the mismatch of blood supply (oxygen delivery) and blood request for adequate oxygenation of tissue.

It is hereby postulated that far infrared radiation of the body will promote blood and oxygen supply to the affected tissues. In addition, the analgesic properties of far infrared will alleviate pain due to the crisis.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 10
Est. completion date January 2009
Est. primary completion date September 2008
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- People with sickle cell disease

Exclusion Criteria:

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Radiation:
Far Infrared Radiation (5µm to 20µm wavelength)
Far infrared radiation for 30 to 40 minutes during each session.

Locations

Country Name City State
Canada The Centre for Incurable Diseases Mississauga Ontario

Sponsors (1)

Lead Sponsor Collaborator
GAAD Medical Research Institute Inc.

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Management 40 minutes No
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