Comparison of Outcome in Neuromuscular Electrical Stimulation Therapy Between Upper and Lower Extremities in Patients with Extracorporeal Membrane Oxygenation Support-Randomized Controlled Trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0008278

Enrollment

Registered

2023-03-07

Start date

2023-03-01

Completion date

Unknown

Last updated

2023-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : - ECMO-applied patients are randomly assigned to upper extremity electrical stimulation treatment group, lower extremity electrical stimulation treatment group, and control group. - E

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1) Patients between the ages of 20 and 90 who are applying ECMO in an intensive care unit (2) Patients who can receive electrical stimulation therapy (3) If you agree to participate in the study

Exclusion criteria

Exclusion criteria: (1) Patients with severe trauma in the area where electrical stimulation treatment is to be performed (2) Patients with unstable vital sign even during ECMO (3) pregnant patients (4) Patients requiring intensive medical management due to uncontrolled internal bleeding (5) Patients suffering from statutory infectious diseases (6) Other researchers judge that the condition of the subject is difficult to participate in the clinical trial

Design outcomes

Primary

Measure	Time frame
ejction fraction	—

Secondary

Measure	Time frame
ICU mobility scale;functional status score for the ICU;physical function in intensive care test scored;Mechanical ventilation application time and type of departure;manual muscle test;functional ambulatory category;ICU length of stay;death or not	—

Countries

Korea, Republic of

Contacts

Public ContactKIM Gahyeon

Chonnam National University Hospital

gahyun5370@naver.com+82-62-220-5186

Outcome results