Summary

Eligibility
for people ages 18-35 (full criteria)
Healthy Volunteers
healthy people welcome
Location
at UCSF
Dates
study started
study ends around

Description

Summary

This study will collect physiological measurements in healthy adult volunteers under controlled hypoxia and hemodilution conditions.

Details

Subjects will undergo stepwise reductions in oxygen saturation and hemoglobin concentration while noninvasive monitoring data are recorded and compared with reference blood measurements.

Keywords

Hypoxia, Hemodilution, Pulse oximetry, Hb, Noninvasive Physiological Monitoring Device

Eligibility

You can join if…

Open to people ages 18-35

  1. In good general health with no evidence of significant medical problems.
  2. Fluent in both written and spoken English.
  3. Has provided written informed consent and is willing to comply with study procedures.

You CAN'T join if...

  1. BMI above 30.
  2. History of heart, lung, kidney, or liver disease.
  3. Diagnosis of asthma, sleep apnea, or use of CPAP.
  4. Diabetes mellitus.
  5. Clotting disorders.
  6. Hemoglobinopathy or history of anemia (ctHb <12 g/dL for men, <11 g/dL for women, COHb >2%).
  7. Any serious systemic illness.
  8. Current smoker.
  9. Injury or abnormality at sensor sites interfering with measurements.
  10. History of fainting or vasovagal response.
  11. Sensitivity to local anesthesia.
  12. Diagnosis of Raynaud's disease.
  13. Unacceptable collateral circulation (Allen's test).
  14. Pregnant, lactating, or attempting to become pregnant.
  15. Unable or unwilling to provide informed consent or comply with study procedures.
  16. Any other condition deemed unsuitable by the investigator.

Location

  • Vital Sign Research Group
    San Francisco California 94107 United States

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
Nihon Kohden
ID
NCT07503171
Study Type
Observational [Patient Registry]
Participants
Expecting 7 study participants
Last Updated