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Scientists probe why sepsis weakens the immune system

NCT ID NCT03788772

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study looks at how certain immune cells, called antigen-presenting cells, behave in people with sepsis—a life-threatening response to infection. Researchers collected blood samples from 119 participants, including sepsis patients, other ICU patients, and healthy volunteers. By analyzing these cells in detail, they hope to understand why sepsis can lead to further infections and poor outcomes.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this study could reveal how sepsis suppresses the immune system, pointing toward new ways to prevent secondary infections.
What could go wrong
This is an observational study, not a treatment trial. It may not lead to direct therapies, and findings may not apply to all sepsis patients.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

119 people

The number who actually took part.

Started

Jul 2019

Finished

Aug 2022

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. ICU patients with severe infections (Sepsis-3 definitions): clinically or microbiologically documented infection and organ dysfunction graded as follows: * Sepsis: increase in the Sequential Organ Failure Assessment (SOFA) score of 2 points or more. * Septic shock: vasopressor requirement to maintain a mean arterial pressure ≥ 65mmHg and serum lactate level \> 2 mmol/L in the absence of hypovolemia 2. ICU patients with non-septic acute circulatory failure: * Cardiogenic shock: left ventricle systolic dysfunction (echocardiographic left ventricular ejection fraction \< 45%) and the need of vasopressor (norepinephrine at any dose and inotropic support (dobutamine ≥ 5 µg/kg/min or epinephrine at any dose) in the absence of patent infection. * Severe hemorrhage: hypotension with acute blood loss requiring transfusion of at least four packed red cells within 24h and vasopressor support by norepinephrine or epinephrine at any dose. 3. Healthy controls: * Blood donors * Patients undergoing elective cataract surgery Exclusion Criteria: 1. All ICU patients * hematological malignancy (or significant history of bone marrow disease), * HIV infection at any stage, * any immunosuppressive drugs including corticosteroids ≥ 0.5 mg/kg equivalent prednisone per day for more 7 days, * anticancer chemotherapy or chemotherapy received during the last three months before inclusion * bone marrow or solid organ transplantation, * leucopenia (\<1000/mm3) excepted if due to sepsis, * pregnancy * do-not-resuscitate order at ICU admission * patients under legal protection regimen. 2. Healthy controls * history of inflammatory disease * hematological malignancy (or significant history of bone marrow disease), * HIV infection at any stage, * any immunosuppressive drugs including corticosteroids ≥ 0.5 mg/kg equivalent prednisone per day for more 7 days, * anticancer chemotherapy or immunotherapy received during the last three months before inclusion * bone marrow or solid organ transplantation, * pregnancy * infectious symptoms within the previous month * subjects under legal protection regimen

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Cochin Hospital, AP-HP

    Paris, 75014, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.