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Evaluation of Respiratory Heast Loss as a Physiologic Patient Monitor for Acute Care Medicine

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ClinicalTrials.gov Identifier: NCT01808963
Recruitment Status : Completed
First Posted : March 12, 2013
Results First Posted : April 8, 2014
Last Update Posted : May 30, 2017
Sponsor:
Information provided by (Responsible Party):
University of California, Davis

Tracking Information
First Submitted Date March 7, 2013
First Posted Date March 12, 2013
Results First Submitted Date July 17, 2013
Results First Posted Date April 8, 2014
Last Update Posted Date May 30, 2017
Study Start Date December 2012
Actual Primary Completion Date June 2013   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: May 27, 2014)
Evaluation of Respiratory Heat Loss as a Physiologic Patient Monitor for Acute Care Medicine [ Time Frame: 1 year. ]
Respired gas heat content
Original Primary Outcome Measures
 (submitted: March 7, 2013)
Evaluation of Respiratory Heat Loss as a Physiologic Patient Monitor for Acute Care Medicine [ Time Frame: 1 year. ]
Measurement of respiratory heat loss in patients undergoing elective surgery.
Change History Complete list of historical versions of study NCT01808963 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Evaluation of Respiratory Heast Loss as a Physiologic Patient Monitor for Acute Care Medicine
Official Title Evaluation of Respiratory Heat Loss as a Physiologic Patient Monitor for Acute Care Medicine
Brief Summary To evaluate the utility of respiratory heat loss measurements as a physiologic monitor.
Detailed Description Respiratory Heat Loss Measured in Joules Per Minute
Study Type Observational
Study Design Observational Model: Case-Only
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population Patient undergoing elective surgery requiring arterial pressure monitoring.
Condition Respiratory Heat Loss
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Actual Enrollment
 (submitted: February 28, 2014)
13
Original Estimated Enrollment
 (submitted: March 7, 2013)
20
Actual Study Completion Date June 2013
Actual Primary Completion Date June 2013   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • Elective surgical procedures.

Exclusion Criteria:

  • Severe pulmonary disease.
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries United States
Removed Location Countries  
 
Administrative Information
NCT Number NCT01808963
Other Study ID Numbers 389048
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party University of California, Davis
Study Sponsor University of California, Davis
Collaborators Not Provided
Investigators
Principal Investigator: Neal W Fleming, M.D., Ph.D Director, Cardiovascular and Thoracic Anesthesiology
PRS Account University of California, Davis
Verification Date May 2017