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NCT Number: NCT06366854

UK ANDROMEDA-Shock-2 RCT

The purpose of the trial is to test if a strategy of resuscitation guided by capillary refill time and individualised clinical hemodynamic phenotyping can improve important clinical outcomes within 28 days in septic shock patients compared to usual care.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Septic shock is a life-threatening condition caused by a severe infection. It can rapidly cause multi-organ failure and is associated with a high risk of dying. Patients with septic shock need emergency treatment with intravenous fluids, antibiotics and medications to improve blood supply to all organs. However, it is clear that giving too much fluid is harmful and giving not enough fluid can make organ failure worse, too. International guidelines exist but there is still a lot of variation in how doctors apply the guideline. Further, it is likely that a "one-size-fits-all" approach does not help all patients.

Previously, the Andromeda-Shock 1 trial showed that resuscitation guided by regular monitoring of skin perfusion was associated with a lower risk of dying than resuscitation guided by regular blood tests. The UK Andromeda-Shock-2 RCT builds on this. The aim is to investigate whether an individualised approach based on monitoring of skin perfusion combined with individualised treatment of the blood pressure and circulation for 6 hours is better for patients with septic shock and reduces the risk of organ failure and dying compared to usual care.

During the study period, the investigators will also take a total of 40ml of blood and 60ml of urine for special kidney tests to evaluate kidney health and recovery of kidney function.

After the study has finished, the investigators plan to share fully anonymised results with the investigators of the international Andromeda Shock 2 trial to get as much information as possible to answer the research question and help patients in future.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Consecutive adult patients (≥ 18 years) with septic shock defined by Sepsis-3 consensus criteria. (ie septic shock defined as suspected or confirmed infection, hyperlactatemia and noradrenaline requirement, after a fluid load of at least 1000mL in 1 hour)

Exclusion criteria

Any of the following criteria preclude participation to the trial:

  • More than 4 hours since septic shock diagnosis,
  • Surgery or acute renal replacement therapy anticipated to start during the 6h intervention period
  • Active bleeding,
  • Child B-C Cirrhosis
  • Underlying disease process with a life expectancy <90 days
  • Attending clinician deems aggressive resuscitation unsuitable
  • Refractory shock (high risk of death within 24h)
  • Pregnancy
  • Concomitant severe acute respiratory distress syndrome
  • Capillary refill time cannot be accurately assessed

Treatment and study plan

Personalised fluid and haemodynamic resuscitation

Procedure

individualised resuscitation

Primary outcomes

  1. hospital mortality

    Time frame: 28 days

    number of patients who died in hospital

  2. organ support

    Time frame: 28 days

    time to cessation of vital organ support

  3. length of stay

    Time frame: 28 days

    length of stay in hospital

Secondary outcomes

  1. mortality

    Time frame: 60 days

    number of patients who died

  2. vital organ support

    Time frame: 28 days

    number of days without vital organ support

  3. length of stay

    Time frame: 60 days

    length of stay in hospital

Study contacts

Contact information is provided by the study sponsor or research team.

Gillian Radcliffe

CONTACT

[email protected]

00442071883036

Marlies Ostermann, PhD

CONTACT

[email protected]

00442071883036

Sponsors and collaborators

Lead sponsor

Guy's and St Thomas' NHS Foundation Trust

Other

Collaborators

  • Pontificia Universidad Catolica de Chile
  • University of Rotterdam, The Netherlands

Registry information

Official study title

Hemodynamic Phenotype-Based, Capillary Refill Time-Targeted Resuscitation In Early Septic Shock: The UK ANDROMEDA-SHOCK-2 Randomized Clinical Trial

Important dates

Study start
2024
Primary completion
2027
Study completion
2028
First posted
Apr 16, 2024
Registry last updated
Jun 20, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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