The Intensive Care Platform Trial

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorAnders Perner

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

10,000 Participants
are divided into 5 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