About this trial
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.
Eligibility criteria
Qualifiers
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.
Disqualifiers
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).
Trial design
Treatments tested in this trial
- Albumin
- No albumin use
- LMWH in weight-adjusted dose
- LMWH in fixed low dose
- LMWH in fixed intermediate dose
Treatment groups
Sponsors and collaborators
Anders Perner
Lead sponsor
Rigshospitalet, Denmark
Sponsor institution
Rigshospitalet, Denmark
Collaborator
Bispebjerg Hospital
Collaborator
Herlev Hospital
Collaborator
Hillerod Hospital, Denmark
Collaborator
Kolding Sygehus
Collaborator
Zealand University Hospital
Collaborator
Slagelse Hospital
Collaborator
Viborg Regional Hospital
Collaborator
Aalborg University Hospital
Collaborator
Aarhus University Hospital
Collaborator
Gødstrup Hospital
Collaborator
Copenhagen University Hospital, Hvidovre
Collaborator
Odense University Hospital
Collaborator
Randers Regional Hospital
Collaborator
University of Copenhagen
Collaborator
North Denmark Region
Collaborator
Region Capital Denmark
Collaborator
Region Zealand
Collaborator
University Medical Center Groningen
Collaborator
Steno Diabetes Center Copenhagen
Collaborator
Karolinska Institutet
Collaborator
Oslo University Hospital
Collaborator
University Hospital, Basel, Switzerland
Collaborator
Tampere University
Collaborator
Collaboration of Research in Intensive Care
Collaborator
Danish Intensive Care Database
Collaborator
The National University Hospital of Iceland
Collaborator