MedDataX Logo

Specialized Treatment, Rehabilitation and Outcome in Patients With Prolonged Critical Illness

NCT ID: NCT04247607

Last Updated: 2022-11-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

250 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-12-13

Study Completion Date

2023-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This prospective observational study aims to describe the outcome for patients with persistent or chronic critical illness treated at Remeo, a clinic specialized for patients in need of prolonged intensive care and intensive care rehabilitation in Sweden. Patients' disease characteristics and the treatment in multidisciplinary patient centered teams for intensive care, weaning from mechanical ventilation and simultaneous rehabilitation will be described. Patients will be followed one year after discharge to document health related quality of life, physical function, frailty, mental illness and used health care resources.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Pulmonary Pathophysiology and Inflammatory Response in Patients Treated With Ecmo for Severe Respiratory Failure

NCT01468142

Respiratory Distress Syndrome, Adult Respiratory Distress Syndrome, Child
COMPLETED

Rehabilitation Practices in Critically Ill Patients Receiving Invasive Mechanical Ventilation in the Intensive Care Unit.

NCT07093125

Mechanical Ventilation Pulmonary Rehabilitation Intensive Care Units (ICUs) +5 more
NOT_YET_RECRUITING

CaRe-ECMO Program on ECMO Weaning

NCT05035797

Critical Illness
RECRUITING NA

Feasibility and Prognosis of Early Rehabilitation in Patients With ECMO

NCT05083624

Extracorporeal Membrane Oxygenation
UNKNOWN NA

Severe ARDS: Generating Evidence

NCT03021824

Acute Respiratory Distress Syndrome Acute Respiratory Failure With Hypoxia Acute Respiratory Failure
COMPLETED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Critical Illness

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Admission to unit (Remeo, Stockholm, Sweden) Treated for prolonged critical illness

Exclusion Criteria

Treated less than 48 hours at unit (Remeo, Stockholm, Sweden)
Minimum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Karolinska Institutet

OTHER

Sponsor Role collaborator

Remeo AB

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Eva Sundman, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Remeo and Karolinska Institutet

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Remeo

Sköndal, Stockholm County, Sweden

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Sweden

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Eva Sundman, MD, PhD

Role: CONTACT

[email protected]
+46702086783

Anna Cedborg, MD, PhD

Role: CONTACT

[email protected]
+46709564216

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Eva Sundman, MD, PhD

Role: primary

[email protected]
+46702086783

Anna Cedborg, MD, PhD

Role: backup

[email protected]
+46709564216

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Dnr 2019-05294

Identifier Type: OTHER

Identifier Source: secondary_id

2019120000

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Feasibility Study of a Home Rehabilitative Network to Treat Prolonged Weaned Patients
NCT01577927 COMPLETED NA
Survival After Failed First-line Non-invasive Ventilation in Acute on Chronic Obstructive Pulmonary Disease
NCT03011853 COMPLETED
ECMO for Critically Ill Patients With Respiratory Failure and/or Circulatory Failure
NCT04031794 UNKNOWN
Diaphragm Protective Ventilation in the Intensive Care Unit
NCT03527797 COMPLETED NA
Extracorporeal Membrane Oxygenation Physical Training
NCT03328767 COMPLETED NA
Nutrition Therapy in Adult Patients Requiring ECMO in Australia and New Zealand
NCT02048046 COMPLETED
Efficacy of Non-Invasive Mechanical Ventilation in Early Hypoxia Secondary to Thoracic Trauma
NCT00557752 TERMINATED PHASE4
Prone Position for Non-intubated Patients With Acute Respiratory Failure
NCT00526981 UNKNOWN NA
Evaluation of Membrane Lung Function in High-altitude Regions
NCT06152744 RECRUITING
Ventilatory Parameters in Acute Neurological Injury
NCT06192342 RECRUITING
Effect of Transpulmonary MP on Prognosis of Patients With Severe ARDS Treated With VV-ECMO
NCT06062212 RECRUITING
Wise Choices in the Intensive Care Unit
NCT07013175 RECRUITING NA
Extracorporeal Membrane Oxygenation for Respiratory Failure Patients
NCT06231446 RECRUITING
IMV to Accelerate Recovery of Lung Function in Veno-venous Extracorporeal Membrane Oxygenation; Lung Rest Or Moderate Mechanical Ventilation in ECMO
NCT06006676 RECRUITING NA
Development of an Early Warning Model for Intensive Care Unit-Acquired Weakness in Mechanically Ventilated Children: A Disease-Specific Cohort and Database Study
NCT07150637 NOT_YET_RECRUITING
Development of a Rehabilitation Strengthening and Mobility Program for Ventilator Dependent Older Patients
NCT03195127 COMPLETED NA
Observational Cohort Study of a National Extracorporeal Membrane Oxygenation Service for Adults With Respiratory Failure: the NHS ECMO Study.
NCT03979222 COMPLETED
Effects on Biotrauma of NMBAs and PP Association During ARDS
NCT06212492 RECRUITING NA
Respiratory Care in Intensive Care Unit for Neuromuscular Patients
NCT02936908 UNKNOWN
Two Modes of Mechanical Ventilation for Intensive Care Patients With Low Blood Oxygen Due to Breathing Difficulties
NCT06140056 TERMINATED NA
Outcome and Predictors of Mortality of Patients on Prolonged Mechanical Ventilation
NCT06087939 NOT_YET_RECRUITING
Safety and Efficacy of Low-Flow ECMO in a Multi-modal Cohort of Adults in Respiratory Failure
NCT06938217 ENROLLING_BY_INVITATION NA
Extracorporeal Membrane Oxygenation for Severe Acute Respiratory Distress Syndrome
NCT01470703 COMPLETED NA
PREdiCtIon of Weanability, Survival and Functional outcomEs After ECLS
NCT05444764 RECRUITING
Towards RECOVER: Outcomes and Needs Assessment in Intensive Care Unit (ICU) Survivors of Prolonged Mechanical Ventilation and Their Caregivers
NCT00896220 UNKNOWN