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NCT04871620Completed

Reliability of a New Pulse Contour Technique for Diagnosing an Increase in Stroke Volume During a Fluid Challenge for Hemodynamic Optimization in Patients Scheduled for High-risk Abdominal Surgery: Comparison With Transthoracic Echocardiography: COMPARE Study

Source: ClinicalTrials.gov · Last updated 18 Jun 2026

Brief summary (registry, in English)

The present study aims at assessing the ability of a new pulse contour device for diagnosing a \>15% stroke volume (SV) increase during patient hemodynamic optimization by fluid challenge in high risk abdominal surgery.

Status (registry)
Completed
Study type
Observational
Enrollment
100 (actual)
First submitted
29 Apr 2021
Start date
12 Apr 2016
Primary completion date
8 Jan 2024
Lead sponsor
Centre Hospitalier Universitaire de Nīmes
Diseases
Stroke
NCT number
NCT04871620

What you commit to

  • Study type: Observational
  • Participants enrolled: 100
  • From 12 Apr 2016 to the primary completion date, 8 Jan 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Cardiac arrythmia
  • Patient in whom the cardiac output monitoring or measurement was not possible by Esophageal Doppler or echography
  • Patients in whom cardiac arrythmia occurred during the procedure of hemodynamic optimization.

Lab values

  • Patients with hemostasis anomaly (PT \< 30%, platelets \< 50 000 elements/mm3)

Other

  • Patient \< 18-year-old
  • Patient with anomaly in oro-pharyngo-esophageal tractus

Who the study is looking for

  • Adult patient ASA status 1-3 who were orally informed and did refuse to participate.
  • Patient in whom general anesthesia with tracheal intubation were planned.
  • Patient in whom an arterial catheter and a monitoring of cardiac output by esophageal Doppler were indicated for hemodynamic optimization
  • Patient with cardiac sinusal mode

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU de Nîmes
Coordinator of this site? Confirm its status
NîmesFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.