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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01981902
Other study ID # 20129075
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date August 2013
Est. completion date August 2018

Study information

Verified date October 2022
Source University of California, Irvine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Dehydration can result from exposure to harsh environments including hot and dry desert climates. Soldiers and non-military workers are frequently required to work in hot, dry conditions, and dehydration can be productivity limiting and life threatening if unrecognized.


Description:

The research can use low power laser technology to take measurements of muscle tissue water content in volunteers before and after marathon training runs to detect dehydration. Two slightly different devices can be used to detect dehydration. 1). diffuse optical spectroscopy and 2). spatial frequency domain imaging-modulated imaging The researchers can determined by use other methods to assess the level of dehydration status in runners. These methods will include taking weight and temperature before and after run, skin-fold measurements pre and post run, and obtaining saliva samples from before and after run. The researchers can determine the study use non-invasive, laser light technology measure tissue water concentrations, as an indicator of dehydration.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date August 2018
Est. primary completion date August 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - male female ages of 18 and 60 - training for a marathon Exclusion Criteria: 1. Poorly controlled diabetes mellitus 2. Diabetes insipidus (excessive urination of water) as diagnosed by your physician 3. disorder of the intestine 4. Irritable bowel syndrome with excessive diarrhea, as diagnosed by a physician 5. Congestive heart failure and subsequent use of a diuretic "water pill" to remove excess water from the body 6. Have poor kidney function 7. Have been diagnosed with hyperthyroidism/hypothyroidism by your physician

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Non-Invasive Optical Spectroscopic
Non-Invasive Optical Spectroscopic

Locations

Country Name City State
United States Beckman Laser Institute University of California Irvine Irvine California

Sponsors (2)

Lead Sponsor Collaborator
University of California, Irvine Beckman Laser Institute University of California Irvine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hydration Marathon Trainees up to 4 weeks
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