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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04918498
Other study ID # 2021-0205
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2021
Est. completion date December 30, 2022

Study information

Verified date May 2021
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Fei Zeng
Phone 13757119536
Email zengfei@zju.edu.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Promote early recovery through the application of early physiotherapy programs for VV-ECMO patients


Description:

This study is intended to construct early physiotherapy programs for VV-ECMO patients, including multidisciplinary team building, safety assessment, early active physiotherapy, respiratory physiotherapy, with a view to promoting early recovery of patients, early withdrawal of ventilator-assisted ventilation, shortening ECMO auxiliary time, improving patients' exercise level and respiratory function, reducing complications, and improving the quality of near-term and long-term survival.


Recruitment information / eligibility

Status Recruiting
Enrollment 34
Est. completion date December 30, 2022
Est. primary completion date September 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - VV-ECMO assisted support - lung failure (e.g. ARDS) - age =18 years - sober - informed consent to this study Exclusion Criteria: - unstable blood flow mechanics - active bleeding - mental disorders that do not work together - people waiting for lung transplants - people at the end of life (e.g. advanced lung cancer)

Study Design


Related Conditions & MeSH terms

  • Extracorporeal Membrane Oxygenation Complication

Intervention

Behavioral:
early physiotherapy programs
establishment of multidisciplinary teams, safety assessment, early activity physiotherapy and respiratory physiotherapy
routine treatment
provide routine nursing and rehabilitation program

Locations

Country Name City State
China SAHZhejiangU Hangzhou Zhejiang

Sponsors (4)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University Changxing Hospital, Jiaxing Second Hospital, Yuhang Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary VV-ECMO auxiliary time the time for VV-ECMO auxiliary 1 year
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