Last reviewed · How we verify

NCT04932330: ICU-AW

Risk Factors of ICU-acquired Weakness

Status unknown Last updated 21 June 2021
What this trial tests

trial in ICU Acquired Weakness in 85 participants. Status unknown.

Timeline
1 March 2017
Primary endpoint
1 March 2020
1 June 2022

Quick facts

Lead sponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment85
Start date1 March 2017
Primary completion1 March 2020
Estimated completion1 June 2022
Sites1 location across China

Conditions studied

Sponsor

Second Affiliated Hospital, School of Medicine, Zhejiang University

Who can join

Adults 18 to 80, any sex, with ICU Acquired Weakness. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

We conducted a retrospective study of critical ill patients who used ECMO during their ICU stay. ICU-AW was diagnosed at the time when patients discharged and had a Medical Research Council (MRC) sum score \< 48 out of a maximal score of 60. We divided patients to ICU-acquired weakness group and no ICU-acquired weakness group and compared their clinical characteristics. Baseline characteristics and therapy details were collected from the case report forms and inspection reports. Univariable analysis and logistic regression analysis were used to analyze clinical characteristics of individuals and to find risk factors of ICU-AW.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for ICU Acquired Weakness

Currently open trials in the same condition.

Other Second Affiliated Hospital, School of Medicine, Zhejiang University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04932330.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing