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Caloric Stimulation on Cerebral Blood Flow

This study has been completed.
Scion NeuroStim
Information provided by (Responsible Party):
Duke University Identifier:
First received: June 26, 2012
Last updated: March 20, 2017
Last verified: June 2015
This is a prospective, non-randomized study designed to generate preliminary data to assess the effect of a new portable non-invasive caloric stimulator on EEG waveform and cerebral blood flow on normal healthy volunteers.

Condition Intervention
Healthy Volunteer Device: ThermoNeuroModulation (TNM) Device

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: The Effect of Vestibular Stimulation on Cerebral Blood Flow

Further study details as provided by Duke University:

Primary Outcome Measures:
  • Changes in cerebral blood flow [ Time Frame: 20 minutes ]
    Changes in cerebral blood flow will be quantified through the use of bilateral transcranial Doppler (TCD). The baseline TCD of three vessels will be compared with measurements taken at 30 second intervals for 5 minutes after caloric stimulation.

Secondary Outcome Measures:
  • Alterations in EEG readings [ Time Frame: 40 minutes ]
    EEG readings occurring between baseline, active CVS induction, and post-CVS induction periods will be assessed to identify and characterize alterations in the readings.

  • Alterations in regional cerebral brain flow (rCBF) [ Time Frame: 40 minutes ]
    A standard noninvasive near infrared spectroscopy system will be used to look for any alterations in rCBF induced by CVS treatment.

Enrollment: 10
Study Start Date: June 2012
Study Completion Date: April 2015
Primary Completion Date: March 2015 (Final data collection date for primary outcome measure)
Intervention Details:
    Device: ThermoNeuroModulation (TNM) Device
    Non-invasive neurostimulator used for up to 20 minutes in a session.
Detailed Description:
Study activities include monitoring with bilateral transcranial Doppler (TCD), EEG and continuous EKG monitoring at 30 second intervals for 5 minutes. This is followed by placement of the caloric stimulator investigational device for 20 minutes. An additional 20 minutes of TCD and EEG monitoring will also be recorded. This will end study participation.

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • no history of neurological disease

Exclusion Criteria:

  • persons under the age of 18
  • pregnant or nursing women
  • history of neurological disease
  • history of psychiatric disease
  • congenital heart defect, known cardiac shunt
  • inner ear or pulmonary disease
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01629901

United States, North Carolina
Duke University Medical Center
Durham, North Carolina, United States, 27710
Sponsors and Collaborators
Duke University
Scion NeuroStim
Principal Investigator: Daniel Laskowitz, MD Duke University
  More Information

Responsible Party: Duke University Identifier: NCT01629901     History of Changes
Other Study ID Numbers: Pro00035775
Study First Received: June 26, 2012
Last Updated: March 20, 2017

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Duke University:
Healthy volunteer processed this record on September 19, 2017