Study Results
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.
UNKNOWN
85 participants
OBSERVATIONAL
2017-03-01
2022-06-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
New Onset Weakness in Critically Ill Patients and the Risk of Death and Recurrent ICU Admission
NCT00106665
Disease Severity, Mortality Risk, and Muscle Function in Intensive Care Unit Patients
NCT07124442
Severe Hypoxemia : Prevalence, Treatment and Outcome
NCT02722031
To Construct a Prognosis Prediction Model for ECMO Patients Based on Machine Learning Algorithms
NCT06654388
Functional Assessment in Critically Ill Patients
NCT07191743
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.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
OTHER
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
ICU-acquired weakness group
Patients receiving extracorporeal membrane oxygenation support who had a Medical Research Council (MRC) sum score \< 48 out of a maximal score of 60 when discharged.
No interventions assigned to this group
no ICU-acquired weakness group
Patients receiving extracorporeal membrane oxygenation support who had a Medical Research Council (MRC) sum score ≥ 48 out of a maximal score of 60 when discharged.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Second Affiliated Hospital, School of Medicine, Zhejiang University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Xinyi Chen
Hangzhou, Please Select, China
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
man huang, phD
Role: CONTACT
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
man huang
Role: backup
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2021-0041
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.