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Comparison of Monitors of Fluid Therapy

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ClinicalTrials.gov Identifier: NCT00286338
Recruitment Status : Completed
First Posted : February 3, 2006
Last Update Posted : January 14, 2009
Sponsor:
Information provided by:
Rigshospitalet, Denmark

Study Description
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Brief Summary:
The investigators want to correlate different methods to guide fluid therapy. The investigators know that guidance by esophagus doppler technique has improved outcome and want to correlate other already used techniques to esophagus doppler.

Condition or disease
Hypovolemia

Detailed Description:

Fluid therapy before and under surgery can be guided by measurement of the hearts ability to eject blood (cardiac output). By doing this it has been shown that the occurrence of nausea,vomiting and complications generally can be reduced. The function of the heart has been measured with a probe in the esophagus in in earlier studies. We want to correlate these results with other techniques by which fluid therapy also is guided in daily practice. These are: SVO2, modelflow (finapres)and NIRS.

These methods are noninvasive except SVO2 measurement which requires a central venous catheter (CVK). Therefore we have chosen a population in which CVK is standard in our institution. We thereby don´t apply any further risks than daily practice and the project is considered as a quality assessment of used standards.

Study Design
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Study Type : Observational
Enrollment : 12 participants
Time Perspective: Prospective
Official Title: Comparison of Monitors of Fluid Therapy
Study Start Date : February 2006
Actual Study Completion Date : April 2006
Groups and Cohorts
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Outcome Measures
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Eligibility Criteria
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Ages Eligible for Study:   18 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age 18 years or older
  • Elective urological surgery in which a central venous catheter is routinely administered
  • Informed consent

Exclusion Criteria:

  • Age 70 years or older
  • No informed consent
  • Pathology in the esophagus that contraindicates use off gastric tube and esophagus doppler
  • ASA III or above
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00286338


Locations
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Denmark
Dept of anesthesia 2041, ABD centre, Rigshospitalet, Blegdamsvej
Copenhagen, Denmark, DK-2100
Sponsors and Collaborators
Rigshospitalet, Denmark
Investigators
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Study Director: Henrik Kehlet, M.D., Ph.D dept of surgical patophysiology
More Information
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ClinicalTrials.gov Identifier: NCT00286338    
Other Study ID Numbers: des.prost-1
First Posted: February 3, 2006    Key Record Dates
Last Update Posted: January 14, 2009
Last Verified: January 2009
Keywords provided by Rigshospitalet, Denmark:
Fluid therapy
Monitoring
Additional relevant MeSH terms:
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Hypovolemia
Pathologic Processes