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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05187273
Other study ID # ID3724
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 25, 2021
Est. completion date December 30, 2023

Study information

Verified date March 2024
Source Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study investigators explore the effects of a dynamic elastance guided protocol compared to a stroke volume variation fluid therapy on lactate levels during major abdominal surgery. Hence investigators created two groups: in the intervention group fluids are given in fluid-responders (SVV > 13%) based on high value of dynamic elastance (ie. Eadyn > 0.9). In the standard group fluids are administered when SVV > 13%.


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date December 30, 2023
Est. primary completion date August 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: patients enrolled for major abdominal surgery - Exclusion Criteria: 1. end-stage renal disease 2. severe heart dysfunction 3. heart rhythm alterations

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Elastance Group
Fluids are given based on dynamic elastane value

Locations

Country Name City State
Italy Andrea Russo Rome

Sponsors (1)

Lead Sponsor Collaborator
Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary lactate levels at the end of surgery
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