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Septic Shock, Vasopressor ResistancePhase 3ADRESSNCT07569536

Efficacy of the Alpha 2 Agonist Dexmedetomidine for Sympathetic Deactivation in REfractory Septic Shock

A Phase 3 study testing Dexmedetomidine 100 µg/mL, intravenous solution and Stardard care in people with Septic Shock, Vasopressor Resistance, run by Hospices Civils de Lyon at 18 sites in France.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Septic shock is one of the most frequent reasons for admission to intensive care units and remains associated with a high mortality rate of approximatively 40% at 28 days. Nearly half of deaths attributable to septic shock occur within the first 3 days and are directly related to the consequences of circulatory… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Septic Shock, Vasopressor Resistance
What is being tested?
Dexmedetomidine 100 µg/mL, intravenous solution and Stardard care
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
360 participants
Where
18 sitesFrance
Study dates
1 Sep 2026to 1 Dec 2028
Phase
Phase 3
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age ≥ 18 years old
  • Septic shock, defined by the "sepsis-3" criteria :
  • oProven or suspected infection, with modification of the SOFA score ≥ 2 points oWith persistent hypotension requiring vasopressors to maintain MAP ≥ 65 mmHg
  • And serum lactate level > 2 mmol/L despite adequate vascular filling
  • Catecholamine resistance, defined by
  • The need for a dose of norepinephrine ≥ 0.5 µg/kg/min for more than 2 consecutive hours
Show all 11Show fewer
  • AND persistence of circulatory failure with at least one of the following criteria present in the 2 hours prior to randomization : hyperlactatemia (> 2 mmol/L) and/or mottling (score ≥ 1) and/or oliguria (diuresis < 0.5 mL/kg/h over the last 2 hours)
  • Adequate vascular filling : ≥ 30 mL/kg OR absence of preload-dependency criteria at time of assessment (passive leg lift, pulsed pressure variation)
  • Invasive mechanical ventilation
  • Patient affiliated to the national heatlh insurance system
  • Written consent from the

Who cannot join

  • Cardiac index < 2.2 L/min/m2 after volume correction
  • Bradycardia < 55 bpm (apart from treatment with ẞ-bloquant) or 2nd or 3rd degree BAV not equipped
  • Patients who are moribund or for whom death appears imminent within 24 hours (as determined by the investigator's clinical judgment
  • Severe hepatic insufficiency with TP and factor < 50% in the absence of DIC (disseminated intravascular coagulationà
  • Hypersensitivity to dexmedetomidine
  • Patient on dexmedetomidine before inclusion
Show all 11Show fewer
  • Patients who received iproniazide within the 15 days preceding randomization
  • Patient for whom a decision has been made to limit the use of therapies
  • Person subject to limited judicial protection or a legal protection measure (curatorship, guardianship)
  • Patients participating in another clinical study with an ongoing exclusion period at the time of inclusion
  • Pregant or breastfeeding woman

Trial locations and contacts

18 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Auguste DARGENT, Doctor contact

+33 4 78 86 20 06

auguste.dargent@chu-lyon.fr

Jean-Pierre QUENOT, Professor contact

+33 3 80 29 37 51

jean-pierre.quenot@chu-dijon.fr

18 sites in 1 country

France18 sites
  • CHU Amiens-Picardie - Service de médecine intensive-réanimation

    Amiens, 80054

    Yoann ZERBIB, MD, +33322088000, zerbib.yoann@chu-amiens.fr

    Yoann ZERBIB, MD

  • Centre Hospitalier Chalon-sur-Saône - Service de réanimation et surveillance continue

    Chalon-sur-Saône, 71321

    Thomas MALDINEY, MD, +333 85 91 01 11, thomas.maldiney@ch-chalon71.fr

    Thomas MALDINEY, MD

  • Centre Hospitalier de Dieppe - Service de réanimation et unité de soins continus

    Dieppe, 76202

    Antoine MARCHALOT, MD, +33232147253, AMarchalot@ch-dieppe.fr

    Antoine MARCHALOT, MD

  • CHU Dijon Bourgogne - Service de médecine intensive et réanimation

    Dijon, 21000

    Jean-Pierre QUENOT, MD, +33380293751, jean-pierre.quenot@chu-dijon.fr

    Jean-Pierre QUENOT, MD

  • APHP - Hôpital Raymond-Poincaré - Service de Médecine intensive-réanimation

    Garches, 92380

    Djillali ANNANE, MD, +331 47 10 77 78, djillali.annane@aphp.fr

    Djillali ANNANE, MD

  • Centre Hospitalier Départemental de Vendée - Service de réanimation polyvalente

    La Roche-sur-Yon, 85925

    Samuel GENSBURGER, MD, +332 51 44 61 61, samuel.gensburger@ght85.fr

    Samuel GENSBURGER, MD

  • Centre Hospitalier Le Mans - Service de réanimation médico-chirurgicale

    Le Mans, 72037

    Jean-Christophe CALLAHAN, MD, +332 43 43 24 58, jccallahan@ch-lemans.fr

    Jean-Christophe CALLAHAN, MD

  • Hôpital Edouard Herriot - Service de Médecine intensive - reanimation

    Lyon, 69003

    Laurent ARGAUD, MD, +334 72 11 28 62, laurent.argaud@chu-lyon.fr

    Laurent ARGAUD, MD

  • Hôpital de la Croix Rousse - Service de médecine intensive et réanimation

    Lyon, 69004

    Louis CHAUVELOT, MD, +33472071762, louis.chauvelot@chu-lyon.fr

    Louis CHAUVELOT, MD

  • Hôpital Saint Joseph Saint Luc - Service de réanimation

    Lyon, 69007

    Emmanuel VIVIER, MD, +334 78 61 88 18, evivier@saintjosephsaintluc.fr

    Emmanuel VIVIER, MD

  • Hôpital de l'archet - Service de médecine intensive et réanimation

    Nice, 06200

    Alan MOUROUGAYEN, MD, +334 92 03 77 77, mourougayen.a@chu-nice.fr

    Alan MOUROUGAYEN, MD

  • Service d'Anesthésie - Médecine Intensive - Réanimation Hôpital Lyon Sud

    Pierre-Bénite, 69310

    Auguste DARGENT, Doctor, +33 4 78 86 20 06, auguste.dargent@chu-lyon.fr

    Auguste DARGENT, MD

  • CHU de Rennes - Service de médecine intensive et réanimation

    Rennes, 35033

    Nicolas TERZI, MD, +33299284321, Nicolas.TERZI@chu-rennes.fr

    Nicolas TERZI, MD

  • Hôpital Nord - CHU Saint Etienne - Service de médecine intensive

    Saint-Priest-en-Jarez, 42270

    Sophie PERINEL, MD, +33477828002, sophie.perinel.ragey@univ-st-etienne.fr

    Sophie PERINEL, MD

  • Nouvel Hôpital Civil - Service de médecine intensive et réanimation

    Strasbourg, 67091

    Julie HELMS, Professor, +333 69 55 04 34, julie.helm@chru-strasbourg.fr

    Julie HELMS, Professor

  • Centre Hospitalier Intercommunal de Toulon - Service de réanimation polyvalente

    Toulon, 83100

    Jonathan CHELLY, MD, +334 94 14 50 00, jonathan.chelly@ch-toulon.fr

    Jonathan CHELLY, MD

  • HOPITAL NORD FRANCHE-COMTE - Service de réanimation

    Trévenans, 90400

    Paul MONASTEROLO, MD, +333 84 98 21 91, PAUL.MONASTEROLO@hnfc.fr

    Paul MONASTEROLO, MD

  • Médipôle Hôpital Privé Lyon Villeurbanne- Service de réanimation polyvalente

    Villeurbanne, 69100

    Stanislas LEDOCHOWSKI, MD, +334 87 65 01 88, sledochowski@scprea.fr

    Stanislas LEDOCHOWSKI, MD

Other trials in France

About this study

Official title: Efficacy of the Alpha 2 Agonist Dexmedetomidine for Sympathetic Deactivation in REfractory Septic Shock: a Randomized, Controlled Trial

Septic shock is one of the most frequent reasons for admission to intensive care units and remains associated with a high mortality rate of approximatively 40% at 28 days. Nearly half of deaths attributable to septic shock occur within the first 3 days and are directly related to the consequences of circulatory failure leading to multiple organ dysfunction. In some patients, persistent shock despite adequate resuscitation leads to early death. This condition is referred to as refractory septic shock. Although its pathophysiology if multifactorial, refractory septic shock is largely characterized by profound vasoplegia and reduced responsiveness to vasopressor therapy.

Current guidelines recommend norepinephrine as the first-line vasopressor. Vasopressin may be considered as a second-line agent, although the addition of vasopressin to norepinephrine has not consistently demonstrated a survival benefit compared with norepinephrine alone. Corticosteroids are also recommended in patients with refractory septic shock with a low level of evidence. Similarly, the addition of other vasopressors such as selepressin or angiotensin II may reduce catecholamine requirements but has not consistently demonstrated an improvement in mortality.

Read more

More recently, a meta-analysis evaluating all non-adrenergic therapeutic strategies confirmed that none of these strategies individually provides a clear mortally benefit. However, when considered collectively, non-adrenergic approaches were associated with improved outcomes in patients with septic shock, supporting the concept that strategies aimed at bypassing or limiting excessive catecholaminergic stimulation may be beneficial in this population.

In parallel, α2-adrenergic agonists are increasingly used as sedative agents in intensive care. Dexmedetomidine has been shown in experimental models to restore vascular responsiveness to vasopressors. Clinical studies conducted in patients with severe sepsis or septic shock have also suggested a potential benefit, including reduced vasopressor requirements and improved hemodynamic stability in the most severely ill patients. Therefore, dexmedetomidine may provide clinically relevant benefits through improved hemodynamic control during the acute phase of septic shock. By restoring vasopressor sensitivity, dexmedetomidine could potentially address an important therapeutic gap in the management of refractory septic shock.

The underlying hypothesis is that the downregulation of adrenergic receptors observed during sepsis may be a direct consequence of sympathetic hyperactivation. Reversal of this phenomenon through "sympathetic deactivation" using α2-agonists may restore vascular responsiveness to vasopressors.

To prepare the ADRESS trial, the investigator's team conducted a multicenter, randomized, double-blind pilot study (ADRESS Pilot). The primary objective of ADRESS Pilot was to assess the effect of dexmedetomidine on vascular responsiveness to phenylephrine in patients with septic shock and vasopressor resistance. Mortality was also evaluated as a secondary outcome. Thirty-two patients were randomized (16 per group). Due to the small sample size, an imbalance in baseline characteristics was observed, with greater vasopressor resistance in the dexmedetomidine group at the time of randomization, even before treatment administration. Patients allocated to the dexmedetomidine group had lower baseline responsiveness to phenylephrine, which limited the comparability of the groups and made the interpretation of the results particularly challenging.

Nevertheless, 30-day and 90-day mortality were not significantly higher in the dexmedetomidine group. No significant differences were observed between groups in the occurrence of bradycardia or in heart rate. Several sensitivity analyses adjusting for baseline imbalances did not demonstrate a clear beneficial effect of dexmedetomidine. However, these findings may reflect insufficient statistical power, given the very small sample size of the study.

Therefore, a larger and adequately powered trial is required to determine whether dexmedetomidine provides a clinical benefit in patients with refractory septic shock.

Based on the results of ADRESS Pilot, the investigator propose to adapt the design of the ADRESS trial to increase the likelihood of detecting a potential treatment effect. Following the pilot study, the scientific committee decided to modify the study design from a double-blind to an open-label trial in order to reduce the risk of excessive sedation resulting from the addition of a sedative drug in patients already receiving continuous sedation. The target population consists of patients with refractory septic shock and a high risk of mortality. These patients are likely to derive the greatest benefit from a sympathetic deactivation strategy using dexmedetomidine in order to improve clinical outcomes.

Being tested
Dexmedetomidine 100 µg/mL, intravenous solution, Stardard care
Keywords
Septic shock, refractory septic shock, sepsis, severe sepsis, intensive care, vasoplegia, vasopressor resistance, dexmedetomidine, alpha-2 adrenergic agonist
Medical subject headings
Shock, Septic, Sepsis, Vasoplegia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Dexmedetomidine 100 µg/mL, intravenous solutionDrug

    Continuous infusion on dexmedetomidine at 0,7 μg/kg/h for 2 hours and then 1 μg/kg/h at fixed dose

  • Stardard careOther

    fluid administration, source control, antibiotic therapy, and substitutive corticosteroid therapy in strict adherence to current guidelines

Study groups in NCT07569536
Study groupRoleWhat they receive
Dexmedetomidine 100 µg/MlExperimentalPatients in the experimental arm will receive a continuous infusion on dexmedetomidine at 0.7 µg/kg/h for the first 2 hours, and then 1 µg/kg/h at fixed dosed, as long as sedation and/or a norepinephrine dose >0.1 µg/kg/min is required, for a maximum duration of 14 days. The dose will be halved 2 hours prior to complete weaning.
Receives: Drug: Dexmedetomidine 100 µg/mL, intravenous solution
Standard careOtherPatients in the standard care arm will receive optimized, protocolized management in strict adherence to current guidelines, particularly regarding fluid administration, source control, antibiotic therapy, and substitutive corticosteroid therapy
Receives: Other: Stardard care

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 30-day mortality

    Vital status at day 30 after randomization.

    Measured: Day 30 after randomization

Secondary outcomes (14)
  1. 72-hour mortality

    Vital status at 72 hours after randomization

    Measured: 72 hours after randomization

  2. Vasopressor exposure

    Cumulative vasopressor dose and peak vasopressor dose expressed as norepinephrine-equivalent dose (NEE score)

    Measured: 6, 12 and 24 hours after randomization

  3. Use of vasopressin or recue therapies

    Proportion of patients requiring vasopressin or any therapy for refractory shock during follow-up

    Measured: From randomization to day 30

  4. Mean arterial pressure (MAP)

    Evolution of mean arterial pressure (MAP) and MAP to norepinephrine-equivalent (Neq) dose ration (MAP/Neq) to assess vasopressor responsiveness

    Measured: Baseline, 6 hours, 12 hours and 24 hours after randomization

  5. Vasopressor-free days

    Number of days without vasopressor therapy during the first 30 days following randomization

    Measured: Day 0 to day 30

  6. Mechanical ventilation-free days

    Number of days without mechanical ventilation during the first 30 days following randomization

    Measured: Day 0 to day 30

  7. Blood lactate concentration

    Arterial blood lactate levels

    Measured: 6 hours, 12 hours and 24 hours after randomization

  8. SOFA score

    Evolution of organ failure assessed using the Sequential Organ Failure Assessment (SOFA) score (minimum 0, maximum 24).

    Measured: Baseline and day 3 after randomization

  9. Cumulative fluid balance

    Difference between total fluid intake and total fluid output

    Measured: Day 0 to day 5

  10. New-onset or persistent atrial fibrillation

    Occurrence of new-onset atrial fibrillation or persistence of atrial fibrillation requiring clinical management.

    Measured: Within 14 days after randomization

  11. ICU and 90-day mortality

    Vital status at Intensive Care Unit (ICU) discharge and at 90 days following randomization.

    Measured: At day 3 and day 90 after randomization

  12. Clinically significant bradycardia

    Occurrence of bradycardia defined as heart rate < 50 bpm requiring therapeutic intervention

    Measured: During the treatment period (until day 30)

  13. Coma-free days

    Number of days without coma up to day 30

    Measured: Day 0 to day 30 or ICU discharge

  14. ICU delirium

    Occurrence of delirium during ICU stay assessed daily using the CAP-ICU in patients with RASS≥ -3

    Measured: Daily until day 30 or ICU discharge

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 May 2026
  2. Study start1 Sep 2026 (estimated)
  3. Primary completion1 Oct 2028 (estimated)
  4. Study completion1 Dec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
A prospective, randomized (1 :1), open-label, parallel-group, multicenter superiority trial comparing an experimental intervention to standard care
Masking
None (open label)
Enrolment
360 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07569536
Sponsor's protocol ID
69HCL25_0485
Other IDs
2025-524122-18-00, 2025
Acronym
ADRESS
Status last verified
Apr 2026
First submitted
22 Apr 2026
Last updated
6 May 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Dexmedetomidine 100 µg/mL, intravenous solution and Stardard care in people with Septic Shock, Vasopressor Resistance, run by Hospices Civils de Lyon at 18 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 11 inclusion and 11 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: opening soon, as of the sponsor's last update on 6 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 18 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.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

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 Auguste DARGENT, Doctor (+33 4 78 86 20 06, auguste.dargent@chu-lyon.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

30-day mortality (time frame: Day 30 after randomization). 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 6 May 2026.

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