Circulatory Failure / Shock StateMETAFRICNCT07255469
Metabolic Fluid Responsiveness in Children
An observational study of Circulatory Failure / Shock State and Fluid Therapy, run by University Hospital, Bordeaux at 8 sites in France.
Trial summary
The investigators aim to validate markers of metabolic fluid-responsiveness in children with acute circulatory failure following cardiac surgery. This would allow physicians to identify which patient could benefit the most from fluid expansion, thus avoiding useless and potentially dangerous fluid expansions that… Read more about this study
- Who is it for?
- Ages 0 days to 15 years
- Conditions the study is for
- Circulatory Failure / Shock State, Fluid Therapy
- How many people
- 110 participants
- Where
- 8 sitesFrance
- Study dates
- 21 Mar 2025to 18 Apr 2027
- How long will I take part?
- 28 Days
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 0 days to 15 years
- All sexes
- No healthy volunteers
- Child
Study population: Patient hospitalized in an intensive care unit after cardiac surgery with a prescription of a 10ml/kg fluid expansion by the physician in charge
Who may be able to join
- Age less than or equal to 15 years old
- Hospitalization in a pediatric intensive care unit after cardiac surgery
- Prescription by the attending physician of a fluid expansion of 10ml/kg
- Prescription of arterial and venous blood gas before and after the volume expansion to help manage acute circulatory failure
- Patient implanted with a functioning arterial line
- Patient implanted with a functioning central venous line in the superior vena cava territory
Who cannot join
- Patient less than 37 weeks' corrected gestational age
- Hemodynamic instability making the delay necessary for any test dangerous
- Supine position contraindicated or deleterious
- Impairment of echocardiographic acoustic window or restless patient making ultrasonography impossible
- Opposition to participate expressed by the patient or by a parent or legal guardian
Trial locations and contacts
8 sites in 1 country. Contact the study team or a site near you to ask about taking part.
8 sites in 1 country
France8 sites, 8 recruiting
- Recruiting
Hôpital Louis Pradel - Hospices Civils de Lyon
Bron, France, 69500
Elodie PERDREAU, MD, +33 4 26 73 93 48 ext. +33, elodie.perdreau@chu-lyon.fr
- Recruiting
Hôpital Jeanne de Flandre - CHU de Lille
Lille, France, 59000
Marguerite LOCKHART, MD, +33 3 20 44 68 79 ext. +33, marguerite.bouron@chu-lille.fr
- Not yet recruiting
Hôpital de la Timone - Assistance Publique - Hôpitaux de Marseille
Marseille, France, 13385
Solène DENANTE, MD, +33 4 13 42 95 15 ext. +33, solene.denante@ap-hm.fr
- Recruiting
Hôpital mère-enfant - CHU de Nantes
Nantes, France, 44093
Pierre BOURGOIN, MD, MSci, +33 2 76 64 36 12 ext. +33, pierre.bourgoin@chu-nantes.fr
- Recruiting
Hôpital Necker-Enfants Malades - Assistance Publique - Hôpitaux de Paris
Paris, France, 75015
Adrien ARSENE, MD, +33 1 44 38 19 03 ext. +33, adrien.arsene@aphp.fr
- Recruiting
Hôpital Cardiologique Haut Lévêque - CHU de Bordeaux
Pessac, France, 33604
Julien GOTCHAC, MD, +33 5 24 54 92 19 ext. +33, julien.gotchac@chu-bordeaux.fr
- Recruiting
Hôpital Felix Guyon - CHU de la Réunion
Saint-Denis, La Réunion, 97400
Yael LEVY, MD, +262-(0)2 62 90 63 90 ext. +262, yael.levy@chu-reunion.fr
- Not yet recruiting
Hôpital des enfants - CHU de Toulouse
Toulouse, France, 31300
Montserrat SIERRE COLOMINA, MD, PhD, +33 5 34 55 84 84 ext. +33, sierracolomina.m@chu-toulouse.fr
About this study
Official title: Parameters Associated With Metabolic Response to Volume Expansion in Children Post-operative of Cardiac Surgery
The investigators aim to validate markers of metabolic fluid-responsiveness in children with acute circulatory failure following cardiac surgery. This would allow physicians to identify which patient could benefit the most from fluid expansion, thus avoiding useless and potentially dangerous fluid expansions that could lead to fluid overload. To this end, The investigators will evaluate the diagnostic accuracy of the ratio of central venous to arterial carbon dioxide tension (Pv-aCO2) to arteriovenous oxygen content (CavO2), a simple biological marker of anaerobic metabolism, for the diagnosis of metabolic fluid responsiveness defined as a significant increase in oxygen consumption (VO2) after fluid expansion.
Read the detailed description
Acute circulatory failure, defined as a mismatch between oxygen delivery and consumption, is a frequent but serious condition in children after cardiac surgery. Fluid expansion is the cornerstone of acute circulatory failure treatment, but several studies have highlighted the adverse effects of excessive fluid expansion. Therefore, it is crucial to assess the individual benefit-risk ratio before each fluid expansion. Currently, finding fluid responsiveness tests is a major issue in intensive care. Usually, fluid responsiveness is defined as a significant improvement in stroke volume after fluid expansion. However, this is an intermediate objective, as the ultimate goal of the treatment is to restore an adequate balance between oxygen delivery and consumption. In adults, a significant proportion of hemodynamically successful volume expansions (i.e. resulting in a significant increase in stroke volume) are in fact metabolically ineffective, as they do not result in a significant increase in VO2. Certain biological parameters indicating anaerobiosis, such as the Pv-aCO2/CavO2 ratio, could be predictive of metabolic fluid responsiveness (e.g. a significant increase in VO2) in these patients. This has never been investigated in children.
The main objective of this study will be to evaluate the diagnostic accuracy of the Pv-aCO2/DAVO2 ratio at baseline for the diagnosis of metabolic fluid responsiveness, in children hospitalized in intensive care after cardiac surgery, for whom a fluid expansion was prescribed by the physician in charge.
The investigators will conduct a non-interventional, multicentric diagnostic accuracy study in French pediatric intensive care units. VO2 will be measured at baseline (e.g. before fluid expansion) and within 1h after fluid expansion by the combination of echocardiographic assessment and both arterial and venous blood gas. Blood gas are routinely measured, in patients already implanted with arterial and central line, to help manage acute circulatory failure. Echocardiography assessment, which is noninvasive and nonradiative, is also a common practice in this situation. Additional simple demographic, hemodynamic and clinical data will be collected at baseline and within 1 hour after fluid expansion, if monitored. No supplemental blood test or invasive parameter will be collected. These data will be collected from standard monitoring and/or from the patient's medical record.
The primary outcome is the diagnostic accuracy (measured by the area under the receiver operating characteristics curve) of the index test (Pv-aCO2/DAVO2 ratio at baseline) for the diagnostic of metabolic fluid responsiveness, defined as a 15% increase in VO2 after fluid expansion compared to baseline (gold standard test).
- VO2 (ml/min/m2) will be measured as follow, at baseline and within 1h after fluid expansion: VO2=(10.CO.DAVO2)/(Body Surface Area)
- DAVO2: difference between arterial and venous oxygen content (measured by blood gas analysis)
- CO: cardiac output, measured by transthoracic echocardiography as the product of heart rate, left ventricular outflow tract surface (from a parasternal long axis view) and left ventricular outflow tract velocity-time integral (from an apical 5-chambers view).
The secondary outcomes are:
- Diagnostic accuracy (AUROC, %) of the following index tests for the diagnosis of metabolic fluid responsiveness: arterial lactate, central venous oxygen saturation, Pv-aCO2.
- Association between fluid expansions induced tissular oxygen saturation variation and metabolic fluid responsiveness.
- Association between metabolic fluid responsiveness and hemodynamic profile (4 categories, depending on the increase of mean arterial pressure and/or stroke volume after fluid expansion)
- Subgroup analysis of the primary outcome: age, type of fluid expansion, circulatory physiology
- Association between baseline clinical data and metabolic fluid responsiveness Study design: non-interventional study of diagnostic accuracy (non-interventional, prospective, multi center). After a prescription of 10 ml/kg volume expansion by the physician in charge, screening for inclusion and exclusion criteria will be performed by an investigator physician. If the patient is included, volume expansion will be delayed for a few minutes (<5 min) while VO2 and the index test are measured. Within one hour after volume expansion, VO2 will be measured once again to evaluate the metabolic response to fluid expansion (gold-standard test).
Inclusion criteria: Age between 0 days and 15 years old; Patient hospitalized in an intensive care unit after cardiac surgery; Prescription of a 10ml/kg fluid expansion by the physician in charge; Prescription of arterial and venous blood gas before and after the volume expansion to help manage acute circulatory failure; Patient implanted with a functioning arterial line; Patient implanted with a functioning central venous line in the superior vena cava territory Exclusion criteria: Patient less than 37 weeks' corrected gestational age; Hemodynamic instability making the delay necessary for any test dangerous; Supine position contraindicated or deleterious; Impairment of echocardiographic acoustic window or restless patient making ultrasonography impossible; Opposition to participate expressed by the patient or by a parent or legal guardian Number of subjects: One hundred and ten patients are needed. This was calculated with the Obuchowski method, with an alpha risk of 0.05, a statistical power of 80%, a ratio "responder/non-responder" of 3, a predicted area under the receiver operating characteristics curve of 0.85 (based on previous studies) with a confidence interval greater than 0.75 which is a classic threshold for clinical pertinence.
Statistical analysis: Comparisons between metabolic "responders" and "non-responders" (to fluid expansion) will be performed with Student's t-test or Mann-Whitney test for continuous variables; or with the Chi-2 test or Fisher's exact test for categorical variables.
Metabolic fluid responsiveness represents the gold standard test. Patients will be classified as metabolic fluid responders in case of at least 15% increase in VO2 after fluid expansion, compared to baseline.
Diagnostic accuracy of the index tests will be explored. As multiple cut-offs of theses index tests can be defined, the investigators will report a receiver operating characteristic (ROC) curve which graphically represents the combination of sensitivity and specificity for each possible test positivity cut-off. The area under the ROC curve informs in a single numerical value about the overall diagnostic accuracy of the index test. The Youden index will also be calculated. The ROC curves of all index tests will be compared using a DeLong test.
A p value less than 0.05 will be considered statistically significant.
- Conditions
- Circulatory Failure / Shock State, Fluid Therapy
- Keywords
- Circulatory failure, Critical Care, Echocardiography, Fluid therapy, Fluid responsiveness, Goal-directed fluid management, oxygen consumption, pediatrics, volume expansion
- Medical subject headings
- Shock
What is being measured
The primary outcome is the main question the study is designed to answer.
Area under the ROC curve (AUROC, %) of baseline Pv-aCO2/DAVO2 ratio to diagnose metabolic fluid
The primary outcome measure of a diagnostic accuracy study is the discriminative ability of an index test (expressed as an area under the ROC curve) to diagnose a condition (defined by a positive gold-standard reference test). In this study:
- The index test is the baseline Pv-aCO2/DAVO2 ratio, i.e. the ratio between the veno-arterial carbon dioxide partial pressure gradient (mmHg) and the difference between arterial and venous oxygen content (ml.dl-1). Oxygen content and carbon dioxide partial pressure are measured by arterial and central venous blood gas analysis.
- The condition is "metabolic fluid responsiveness"
- The gold-standard reference test to diagnose metabolic fluid responsiveness is a VO2 increase of at least 15% between baseline and after volume expansion (i.e. ((VO2 after volume expansion - VO2 at baseline) / VO2 at baseline) > 15%). VO2 (ml/min/m2) will be measured as follow: VO2=(10.CO.DAVO2)/(Body Surface Area), where CO (ml.min-1) is the cardiac output, measured b
Measured: at baseline
Secondary outcomes (6)
AUROC (%) of the following index test to diagnose metabolic fluid responsiveness (same definition as above )
Baseline arterial lactate (mmol.L-1), from an arterial blood gas analysis
Measured: at baseline
AUROC (%) of the following index test to diagnose metabolic fluid responsiveness (same definition as above )
Baseline central venous oxygen saturation (%), from a central venous blood gas analysis
Measured: at baseline
AUROC (%) of the following index test to diagnose metabolic fluid responsiveness (same definition as above )
Baseline Pv-aCO2 (mmHg), from an arterial and central venous blood gas analysis
Measured: at baseline
Subgroup analysis of the primary outcome
age, type of fluid expansion, circulatory physiology
Measured: at baseline
Correlation between metabolic fluid responsiveness and the following
- Age (0 - 2 years / 2 - 5 years / 5 - 15 years)
- Sex
- Weight
- Number of fluid expansion during the last 24 h
- Baseline Heart rate
- Baseline arterial pressure
- Baseline urine output
- Baseline capillary refill time
- Baseline mottling
- Baseline left atrial pressure, if monitored as usual care
- Baseline PELODS2 score
- Type of volume expansion (albumin or crystalloid)
- % of increase in cerebral near-infrared regional spectrophotometry (NIRS, %) ( baseline / after volume expansion)
- % of increase in systemic near-infrared regional spectrophotometry (NIRS, %) ( baseline / after volume expansion)
- % of increase in mean perfusion pressure (i.e. difference between mean arterial pressure and central venous pressure) ( baseline / after volume expansion)
- % of increase in central venous pressure ( baseline / after volume expansion)
- Hemodynamic profile
Measured: at baseline
Correlation between metabolic fluid responsiveness and the following
- Length of mechanical ventilation (days), evaluated 28 days after inclusion
- Intensive care unit length of stay (days), evaluated 28 days after inclusion.
- Mortality at 28 days after inclusion
Measured: at baseline , 28 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Dec 2025
- Study start21 Mar 2025
- Primary completion21 Mar 2027 (estimated)
- Study completion18 Apr 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Circulatory Failure / Shock StateStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 110 participants (estimated)
- Target duration
- 28 Days
Sponsor and investigators
- Lead sponsor
- University Hospital, Bordeaux
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Julien GOTCHAC, MD, Study director, CHU de Bordeaux - Hôpital Cardiologique Haut Lévêque
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07255469
- Sponsor's protocol ID
- CHUBX 2024/87
- Other IDs
- 2024-A02561-46
- Acronym
- METAFRIC
- Status last verified
- Nov 2025
- First submitted
- 1 Sep 2025
- Last updated
- 1 Dec 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 1 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Parameters Associated With Metabolic Response to Volume Expansion in Children Post-operative of Cardiac Surgery
- ClinicalTrials.gov ID
- NCT07255469
- Acronym / sponsor ID
- METAFRIC / CHUBX 2024/87
- Conditions
- Circulatory Failure / Shock State, Fluid Therapy
- Keywords
- Circulatory failure, Critical Care, Echocardiography, Fluid therapy, Fluid responsiveness, Goal-directed fluid management, oxygen consumption, pediatrics
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 110 participants (estimated)
- Lead sponsor
- University Hospital, BordeauxUniversity, hospital or other
- Study start
- 21 Mar 2025 (actual)
- Primary completion
- 21 Mar 2027 (estimated)
- Study completion
- 18 Apr 2027 (estimated)
- First posted
- 1 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The investigators aim to validate markers of metabolic fluid-responsiveness in children with acute circulatory failure following cardiac surgery. This would allow physicians to identify which patient could benefit the most from fluid expansion, thus avoiding useless and potentially dangerous fluid expansions that could lead to fluid overload. To this end, The investigators will evaluate the diagnostic accuracy of the ratio of central venous to arterial carbon dioxide tension (Pv-aCO2) to arteriovenous oxygen content (CavO2), a simple biological marker of anaerobic metabolism, for the diagnosis of metabolic fluid responsiveness defined as a significant increase in oxygen consumption (VO2) after fluid expansion.
Detailed description
Acute circulatory failure, defined as a mismatch between oxygen delivery and consumption, is a frequent but serious condition in children after cardiac surgery. Fluid expansion is the cornerstone of acute circulatory failure treatment, but several studies have highlighted the adverse effects of excessive fluid expansion. Therefore, it is crucial to assess the individual benefit-risk ratio before each fluid expansion. Currently, finding fluid responsiveness tests is a major issue in intensive care. Usually, fluid responsiveness is defined as a significant improvement in stroke volume after fluid expansion. However, this is an intermediate objective, as the ultimate goal of the treatment is to restore an adequate balance between oxygen delivery and consumption. In adults, a significant proportion of hemodynamically successful volume expansions (i.e. resulting in a significant increase in stroke volume) are in fact metabolically ineffective, as they do not result in a significant increase in VO2. Certain biological parameters indicating anaerobiosis, such as the Pv-aCO2/CavO2 ratio, could be predictive of metabolic fluid responsiveness (e.g. a significant increase in VO2) in these patients. This has never been investigated in children.
The main objective of this study will be to evaluate the diagnostic accuracy of the Pv-aCO2/DAVO2 ratio at baseline for the diagnosis of metabolic fluid responsiveness, in children hospitalized in intensive care after cardiac surgery, for whom a fluid expansion was prescribed by the physician in charge.
The investigators will conduct a non-interventional, multicentric diagnostic accuracy study in French pediatric intensive care units. VO2 will be measured at baseline (e.g. before fluid expansion) and within 1h after fluid expansion by the combination of echocardiographic assessment and both arterial and venous blood gas. Blood gas are routinely measured, in patients already implanted with arterial and central line, to help manage acute circulatory failure. Echocardiography assessment, which is noninvasive and nonradiative, is also a common practice in this situation. Additional simple demographic, hemodynamic and clinical data will be collected at baseline and within 1 hour after fluid expansion, if monitored. No supplemental blood test or invasive parameter will be collected. These data will be collected from standard monitoring and/or from the patient's medical record.
The primary outcome is the diagnostic accuracy (measured by the area under the receiver operating characteristics curve) of the index test (Pv-aCO2/DAVO2 ratio at baseline) for the diagnostic of metabolic fluid responsiveness, defined as a 15% increase in VO2 after fluid expansion compared to baseline (gold standard test).
- VO2 (ml/min/m2) will be measured as follow, at baseline and within 1h after fluid expansion: VO2=(10.CO.DAVO2)/(Body Surface Area)
- DAVO2: difference between arterial and venous oxygen content (measured by blood gas analysis)
- CO: cardiac output, measured by transthoracic echocardiography as the product of heart rate, left ventricular outflow tract surface (from a parasternal long axis view) and left ventricular outflow tract velocity-time integral (from an apical 5-chambers view).
The secondary outcomes are:
- Diagnostic accuracy (AUROC, %) of the following index tests for the diagnosis of metabolic fluid responsiveness: arterial lactate, central venous oxygen saturation, Pv-aCO2.
- Association between fluid expansions induced tissular oxygen saturation variation and metabolic fluid responsiveness.
- Association between metabolic fluid responsiveness and hemodynamic profile (4 categories, depending on the increase of mean arterial pressure and/or stroke volume after fluid expansion)
- Subgroup analysis of the primary outcome: age, type of fluid expansion, circulatory physiology
- Association between baseline clinical data and metabolic fluid responsiveness Study design: non-interventional study of diagnostic accuracy (non-interventional, prospective, multi center). After a prescription of 10 ml/kg volume expansion by the physician in charge, screening for inclusion and exclusion criteria will be performed by an investigator physician. If the patient is included, volume expansion will be delayed for a few minutes (<5 min) while VO2 and the index test are measured. Within one hour after volume expansion, VO2 will be measured once again to evaluate the metabolic response to fluid expansion (gold-standard test).
Inclusion criteria: Age between 0 days and 15 years old; Patient hospitalized in an intensive care unit after cardiac surgery; Prescription of a 10ml/kg fluid expansion by the physician in charge; Prescription of arterial and venous blood gas before and after the volume expansion to help manage acute circulatory failure; Patient implanted with a functioning arterial line; Patient implanted with a functioning central venous line in the superior vena cava territory Exclusion criteria: Patient less than 37 weeks' corrected gestational age; Hemodynamic instability making the delay necessary for any test dangerous; Supine position contraindicated or deleterious; Impairment of echocardiographic acoustic window or restless patient making ultrasonography impossible; Opposition to participate expressed by the patient or by a parent or legal guardian Number of subjects: One hundred and ten patients are needed. This was calculated with the Obuchowski method, with an alpha risk of 0.05, a statistical power of 80%, a ratio "responder/non-responder" of 3, a predicted area under the receiver operating characteristics curve of 0.85 (based on previous studies) with a confidence interval greater than 0.75 which is a classic threshold for clinical pertinence.
Statistical analysis: Comparisons between metabolic "responders" and "non-responders" (to fluid expansion) will be performed with Student's t-test or Mann-Whitney test for continuous variables; or with the Chi-2 test or Fisher's exact test for categorical variables.
Metabolic fluid responsiveness represents the gold standard test. Patients will be classified as metabolic fluid responders in case of at least 15% increase in VO2 after fluid expansion, compared to baseline.
Diagnostic accuracy of the index tests will be explored. As multiple cut-offs of theses index tests can be defined, the investigators will report a receiver operating characteristic (ROC) curve which graphically represents the combination of sensitivity and specificity for each possible test positivity cut-off. The area under the ROC curve informs in a single numerical value about the overall diagnostic accuracy of the index test. The Youden index will also be calculated. The ROC curves of all index tests will be compared using a DeLong test.
A p value less than 0.05 will be considered statistically significant.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 28 Days
Who may qualify
- Ages
- 0 days to 15 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
- Study population
- Patient hospitalized in an intensive care unit after cardiac surgery with a prescription of a 10ml/kg fluid expansion by the physician in charge
Key inclusion criteria (6 listed)
- Age less than or equal to 15 years old
- Hospitalization in a pediatric intensive care unit after cardiac surgery
- Prescription by the attending physician of a fluid expansion of 10ml/kg
- Prescription of arterial and venous blood gas before and after the volume expansion to help manage acute circulatory failure
- Patient implanted with a functioning arterial line
Key exclusion criteria (5 listed)
- Patient less than 37 weeks' corrected gestational age
- Hemodynamic instability making the delay necessary for any test dangerous
- Supine position contraindicated or deleterious
- Impairment of echocardiographic acoustic window or restless patient making ultrasonography impossible
- Opposition to participate expressed by the patient or by a parent or legal guardian
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Area under the ROC curve (AUROC, %) of baseline Pv-aCO2/DAVO2 ratio to diagnose metabolic fluid
Time frame: at baseline
The primary outcome measure of a diagnostic accuracy study is the discriminative ability of an index test (expressed as an area under the ROC curve) to diagnose a condition (defined by a positive gold-standard reference test). In this study: * The index test is the baseline Pv-aCO2/DAVO2 ratio, i.e. the ratio between the veno-arterial carbon dioxide partial pressure gradient (mmHg) and the difference between arterial and venous oxygen content (ml.dl-1). Oxygen content and carbon dioxide partial pressure are measured by arterial and central venous blood gas analysis. * The condition is "metabolic fluid responsiveness" * The gold-standard reference test to diagnose metabolic fluid responsiveness is a VO2 increase of at least 15% between baseline and after volume expansion (i.e. ((VO2 after volume expansion - VO2 at baseline) / VO2 at baseline) > 15%). VO2 (ml/min/m2) will be measured as follow: VO2=(10.CO.DAVO2)/(Body Surface Area), where CO (ml.min-1) is the cardiac output, measured b
6 secondary outcomes
AUROC (%) of the following index test to diagnose metabolic fluid responsiveness (same definition as above )
Time frame: at baseline
AUROC (%) of the following index test to diagnose metabolic fluid responsiveness (same definition as above )
Time frame: at baseline
AUROC (%) of the following index test to diagnose metabolic fluid responsiveness (same definition as above )
Time frame: at baseline
Subgroup analysis of the primary outcome
Time frame: at baseline
Correlation between metabolic fluid responsiveness and the following
Time frame: at baseline
Correlation between metabolic fluid responsiveness and the following
Time frame: at baseline , 28 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Dec 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Julien GOTCHAC, MD study director
CHU de Bordeaux - Hôpital Cardiologique Haut Lévêque
8 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Circulatory Failure / Shock State and Fluid Therapy, run by University Hospital, Bordeaux at 8 sites in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 1 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 8 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Julin GOTCHAC, MD (+33 5 24 54 92 19 ext. +33, julien.gotchac@chu-bordeaux.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Area under the ROC curve (AUROC, %) of baseline Pv-aCO2/DAVO2 ratio to diagnose metabolic fluid (time frame: at baseline). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Dec 2025.