Actively Recruiting
The Intensive Care Platform Trial (INCEPT)
Led by Anders Perner · Updated on 2026-03-19
10000
Participants Needed
21
Research Sites
N/A
Total Duration
On this page
Sponsors
A
Anders Perner
Lead Sponsor
R
Rigshospitalet, Denmark
Collaborating Sponsor
AI-Summary
What this Trial Is About
Among critically ill patients, many die, and many of the survivors and their family members struggle for years with reduced quality of life. Critically ill patients are treated in intensive care units (ICUs). Here, they receive life support, e.g., mechanical ventilation and advanced support of the circulation (heart and blood vessels) and kidneys. In addition, ICU patients receive many other treatments. It is, however, uncertain if all the treatments provide value for the patients. The desirable effects of many treatments are uncertain, and some may be wasteful or even harmful. Clinical trials are necessary to validly assess the desirable and undesirable effects of different treatments. However, conventional clinical trials have limitations: * They typically only assess a single question related to a single comparison of treatments at a time. * They are often not very flexible, including with regards to the number of participants needed, and this increases the risk that a trial will end up as inconclusive. * There is no or limited re-use or sharing of infrastructure across trials, leading to duplicate work and resource use. * Trial participants do usually not benefit from the obtained knowledge before the trial concludes. * Involvement of patients, family members, and other stakeholders is typically limited, which may decrease the relevance of the questions addressed. With the Intensive Care Platform Trial (INCEPT), we aim to tackle these challenges by establishing a flexible platform trial that continuously learns from the obtained results. The platform trial may run forever with simultaneous and continuous assessment of many treatments. INCEPT will continuously learn from the accrued data and use these to improve the treatment of both participating and future patients. With INCEPT, we are also building a framework for thorough and extensive involvement of key stakeholders, including patients and family members. INCEPT will improve the way clinical trials are done and increase the probabilities that treatments are improved. This will: * Directly improve outcomes for ICU patients. * Relieve a strained healthcare system by discarding inefficient or harmful treatments. * Ensure that new treatments are beneficial or cost-effective before implementation. * Lower the costs and burdens of assessing more treatments in the critically ill.
CONDITIONS
Brief Title
The Intensive Care Platform Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
The general eligibility criteria below apply to INCEPT as a whole and thus to all domains. Domains may impose domain-specific eligibility criteria that restrict the population eligible for that domain further, but domains are not allowed to broaden the general eligibility criteria. Domain-specific eligibility criteria always apply to all arms in a domain.
PLATFORM INCLUSION CRITERIA:
- Adult patient (≥18 years old) acutely admitted to the ICU. This includes ICU admissions after emergency surgery, unplanned ICU admissions after elective surgery, and prolonged ICU admissions due to complications after elective surgery (i.e., admissions occurring or being prolonged due to an unexpected, worsened condition, but excluding planned ICU admissions after elective surgery without clinical deterioration).
- Eligible for at least one active domain.
PLATFORM EXCLUSION CRITERIA:
- Informed consent following inclusion expected to be unobtainable (e.g., known previous objections to participation).
- Patient is under coercive measures (e.g., ongoing involuntary hospital stay or under the jurisdiction of correctional authorities).
Patients who have previously been included in INCEPT may only be included again during new ICU admissions but may only be randomised to domains in which they have not previously been randomised.
DOMAIN-SPECIFIC ELIGIBLE CRITERIA:
Each domain may have additional eligibility criteria. Refer to the study website for more information (www.incept.dk).
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 21 locations
1
Anaesthesia, Hospital Sønderjylland
Aabenraa, Denmark, 6200
Not Yet Recruiting
2
Department of Anaesthesia and Intensive Care, Aalborg University Hospital
Aalborg, Denmark, 9000
Actively Recruiting
3
Department of Intensive Care Nord , Aarhus University Hospital
Aarhus, Denmark, 8200
Actively Recruiting
4
Department of Intensive Care Øst, Aarhus University Hospital
Aarhus, Denmark, 8200
Actively Recruiting
5
Department of Cardiothoracic Anaesthesia and Intensive care, Copenhagen Universisty Hospital - Rigshospitalet
Copenhagen, Denmark, 2100
Not Yet Recruiting
6
Department of Intensive Care, Copenhagen University Hospital - Rigshospitalet
Copenhagen, Denmark, 2100
Actively Recruiting
7
Neuroanaesthesiology, Copenhagen University Hospital - Rigshospitalet
Copenhagen, Denmark, 2100
Not Yet Recruiting
8
Department of anesthesiology and intensive care, Bispebjerg-Frederiksberg Hospital
Copenhagen, Denmark, 2400
Actively Recruiting
9
Esbjerg Hospital
Esbjerg, Denmark, 6700
Not Yet Recruiting
10
Department of Anesthesiology and Intensive Care, Copenhagen University Hospital Herlev
Herlev, Denmark, 2730
Not Yet Recruiting
11
Department of Anaesthesiology and Intensive Care, Gødstrup Hospital
Herning, Denmark, 7400
Actively Recruiting
12
Department of Anaesthesia and Intensive Care Medicine, Copenhagen University Hospital - North Zealand
Hillerød, Denmark, 3400
Actively Recruiting
13
Anaesthesiology and Intensive Care, Amager and Hvidovre Hospital
Hvidovre, Denmark, 2650
Actively Recruiting
14
Department of Anesthesia and intensive care medicine, Kolding Hospital
Kolding, Denmark, 6000
Actively Recruiting
15
Department of Anesthesia, Zealand University Hospital
Køge, Denmark, 4600
Actively Recruiting
16
Anesthesiology (ICU), Zealand University Hospital, Nykøbing Falster
Nykøbing Falster, Denmark, 4800
Not Yet Recruiting
17
Department of Anesthesiology and Intensive Care, Odense University Hospital
Odense, Denmark, 5000
Actively Recruiting
18
Operation og Intensiv, Regional Hospital Randers
Randers, Denmark, 8930
Actively Recruiting
19
Intensive care, Slagelse Hospital
Slagelse, Denmark, 4200
Actively Recruiting
20
Department. of Anesthesiology and Intensive Care Medicine
Svendborg, Denmark, 5700
Actively Recruiting
21
Department of Anaesthesiology and Intensive Care, Regional Hospital Viborg
Viborg, Denmark, 8800
Actively Recruiting
Research Team
A
Anders Perner, Professor
M
Morten H Moeller, Professor
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
5
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