Cardiovascular Effects of Norepinephrine

NCT ID: NCT05761522

Last Updated: 2024-08-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

49 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-04-21

Study Completion Date

2025-12-21

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Previous studies of our team reported the improvement of myocardial contractility both on hemodynamic parameters (by transpulmonary thermodilution) and morphological (by transthoracic echocardiography: TTE), during the early phase of septic shock (during the first 4 hours management of septic shock).

However, one can wonder about the effect of NAD on myocardial cardiac ouput and contractility beyond the early phase of septic shock, more precisely beyond the first 24 hours. Indeed, while it continues to act on the "stressed" blood volume and the diastolic left ventricular perfusion by increasing the diastolic arterial pressure (DAP), it has been reported in old studies that beyond the early phase, the sensitivity of the β1-adrenergic receptors is altered due to the phenomenon of internalization of these receptors, leading to a reduction of the myocardial response to catecholamines.

The investigators can then wonder whether norepinephrine still exerts a positive effect on myocardial contractility via the increase in DAP, despite an alteration of the β1-adrenergic pathway.

To answer this question, the investigators proposed to evaluate the effects of norepinephrine by TTE on cardiac contractility after the initial phase.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Patients presenting with septic shock for 24 hours or more and meeting the inclusion criteria may be included.

The course of the study will be as follows:

T0: collection (as part of usual care) of clinical circulatory parameters (heart rate, systolic/diastolic/mean blood pressure) and biological parameters (arterial lactate and ScVo2) and performance of echocardiography.

Parameters collected during TTE:

* Concerning the main judgment criterion and the secondary judgment criteria:

* Left ventricular ejection fraction (LVEF) by the Simpson Biplane method,
* Cardiac output and cardiac index by continuity equation (measurement of left ventricular outflow chamber (mm) and sub-aortic time-velocity integral (cm/s)).
* Tricuspid Annular Systolic Excursion (TAPSE) (mm)
* S wave at the tricuspid ring (cm/s)
* Other parameters collected systematically:

* Surface of the left ventricle (end-systolic and end-diastolic),
* Global strain of the left ventricle
* Mitral Annular Plane Systolic Excursion (MAPSE) (mm)
* Left ventricular filling pressure (LVRP) (at the mitral annulus, E, A, e', S' waves, E/A ratio, E/e');
* Maximum tricuspid regurgitation velocity (m/s) to estimate systolic pulmonary arterial pressure (PAPs) (mmHg)

T1: After the clinician in charge introduces or increases norepinephrine to achieve MAP ≥ 65mmHg, T1 will be when the goal of MAP ≥ 65mmHg is reached. This will be the target MAP for the management of septic shock of the patient in question according to the recommendations of learned societies.

Collection of clinical and biological circulatory parameters and performance of the TTE. The parameters collected will be the same as at T0.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Septic Shock

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Patients with septic shock for 24 hours or more

Adult patients suffering from septic shock, after 24 hours of their diagnosis. Presenting with Mean arterial pressure (MAP)\<65 mmHg or the target MAP For whom the physician in charge decided to increase the norepinephrine dose

transthoracic echocardiography

Intervention Type OTHER

* Concerning the main judgment criterion and the secondary judgment criteria:

* Left ventricular ejection fraction (LVEF) by the Simpson Biplane method,
* Cardiac output and cardiac index by continuity equation (measurement of left ventricular outflow chamber (mm) and sub-aortic time-velocity integral (cm/s)).
* Tricuspid Annular Systolic Excursion (TAPSE) (mm)
* S wave at the tricuspid ring (cm/s)
* Other parameters collected systematically:

* Surface of the left ventricle (end-systolic and end-diastolic),
* Global strain of the left ventricle
* Mitral Annular Plane Systolic Excursion (MAPSE) (mm)
* Left ventricular filling pressure (LVRP) (at the mitral annulus, E, A, e', S' waves, E/A ratio, E/e');
* Maximum tricuspid regurgitation velocity (m/s) to estimate systolic pulmonary arterial pressure (PAPs) (mmHg)

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

transthoracic echocardiography

* Concerning the main judgment criterion and the secondary judgment criteria:

* Left ventricular ejection fraction (LVEF) by the Simpson Biplane method,
* Cardiac output and cardiac index by continuity equation (measurement of left ventricular outflow chamber (mm) and sub-aortic time-velocity integral (cm/s)).
* Tricuspid Annular Systolic Excursion (TAPSE) (mm)
* S wave at the tricuspid ring (cm/s)
* Other parameters collected systematically:

* Surface of the left ventricle (end-systolic and end-diastolic),
* Global strain of the left ventricle
* Mitral Annular Plane Systolic Excursion (MAPSE) (mm)
* Left ventricular filling pressure (LVRP) (at the mitral annulus, E, A, e', S' waves, E/A ratio, E/e');
* Maximum tricuspid regurgitation velocity (m/s) to estimate systolic pulmonary arterial pressure (PAPs) (mmHg)

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Adult patients \>18 years old
* Septic shock after 24 hours from its diagnosis
* MAP\<65 mmHg for which the physician in charge decided to increase NE

Exclusion Criteria

* Patient under Dobutamine
* Pregnancy
* Do not resuscitation decision
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

CHU de Reims

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Chu Reims

Reims, , France

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

France

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Olfa Hamzaoui

Role: CONTACT

3 10 73 69 73 ext. 0033

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Damien JOLLY

Role: primary

326788472 ext. 33

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

PZ23020*

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.