NCT05728359Recruiting
Genomic Determinants of Outcome in Cardiogenic Shock
Prospective Observational Study Investigating Genomic Determinants of Outcome From Cardiogenic Shock (GOlDilOCS)
Source: ClinicalTrials.gov · Last updated 18 Nov 2025
Brief summary (registry, in English)
The aim of this project is to understand the heterogeneity of both the immune consequences and treatment responses in CS. We will explore this heterogeneity through identification of transcriptomic sub-phenotypes and their association with outcomes, including therapeutic responses.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 300 (estimated)
- First submitted
- 22 Sept 2022
- Start date
- Aug 2022
- Primary completion date
- Nov 2026
- Lead sponsor
- Barts & The London NHS Trust
- NCT number
- NCT05728359
What you commit to
- Study type: Observational
- Planned participants: 300
- From Aug 2022 to the primary completion date, Nov 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Age
- Any of the inclusion criteria not met and:
- Unwilling to provide informed consent.
- Echocardiographic evidence (recorded within 90 mins of end of PCI procedure) of mechanical cause for CS: eg ventricular septal defect, LV-free wall rupture, ischaemic mitral regurgitation.
- Age \<18 and ≥80 years.
- Shock from another cause (sepsis, haemorrhagic/hypovolaemic shock, anaphylaxis, etc).
- Significant systemic illness
- Known dementia of any severity
- Comorbidity with life expectancy \<12 months.
- Out-of-hospital cardiac arrest (OHCA) and any of the following:
- No return of spontaneous circulation (ongoing resuscitation effort)
- pH \<7
- Without bystander CPR within 10 minutes of collapse
- Arterial lactate level of \<2.0 mmol per litre.
Who the study is looking for
- All of the following are required for inclusion following screening:
- Willing to provide informed consent or appropriate consent from a nominated consultee or personal consultee
- Presentation within 24 hours of onset of ACS symptoms.
- CS can only be secondary to ACS (Type 1 MI STEMI or N-STEMI) or myocarditis
- Planned or completed revascularisation of culprit coronary artery
- CS will be defined by:
- Systolic blood pressure \<90 mmHg for at least 30 minutes
- A requirement for a continuous infusion of vasopressor or inotropic therapy to maintain systolic blood pressure \> 90 mmHg.
- Clinical signs of pulmonary congestion, plus signs of impaired organ perfusion with at least one of the following manifestations:
- altered mental status.
- cold and clammy skin and limbs.
- oliguria with a urine output of less than 30 ml per hour.
- elevated arterial lactate level of \>2.0 mmol per litre.
Age in the registry: 18 years to 80 years · Sex: All
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Barts Health NHS Trust Coordinator of this site? Confirm its status | London | United Kingdom | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.