Status:
COMPLETED
Echocardiographic Assessment of Volume Variation Secondary to Preoperative Fasting
Lead Sponsor:
Centre Hospitalier Universitaire de Nīmes
Conditions:
Hypovolemia
Eligibility:
All Genders
18-90 years
Brief Summary
The primary objective of this study is to demonstrate that preoperative fasting does not increase the rate of lowered blood volume (defined by a variation of 15% ΔITV during a leg lift) in patients un...
Eligibility Criteria
Inclusion
- The patient must have given his/her informed and signed consent
- The patient must be insured or beneficiary of a health insurance plan
- The patient is ASA (American Society of Anesthesiologists) class I, II or III
- The patient has not been fasting for more than 6 hours at the time of inclusion
- The patient is schelduled for a gynecological or visceral surgery
Exclusion
- The patient is participating in another study
- The patient is in an exclusion period determined by a previous study
- The patient is under judicial protection, under tutorship or curatorship
- The patient refuses to sign the consent
- It is impossible to correctly inform the patient
- The patient is pregnant
- The patient is breastfeeding
- The patient is ASA class IV
- The patient has insulin dependent diabetes
- The patient has a cardiac or respiratory dysfunction
- The patient has a heart rhythm disorder
- The patient has renal insufficiency with dialysis
- The patient is being treated with diuretics
- The patient has had a bowel preparation
- Emergency surgery
- Outpatient surgery
Key Trial Info
Start Date :
January 1 2011
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
April 13 2011
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT01258361
Start Date
January 1 2011
End Date
April 13 2011
Last Update
November 17 2025
Active Locations (1)
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1
Centre Hospitalier Universitaire de Nîmes
Nîmes, Gard, France, 30029