VIDD
Conditions
Interventions
Control group:Under the premise of patients receiving standard treatment within the ICU, engage in routine rehabilitation treatment tailored to the individual patient s condition. The rehabilitation p
Experimental Group:On the basis of the patient s conventional rehabilitation, the patient will undergo electroacupuncture stimulation therapy. The acupoints selected for electroacupuncture stimulation
Sponsors
The 2nd affilated Hospital of Harbin Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: ?Patients Age > 18 years old.?The patient or their family members must voluntarily agree to acupuncture and moxibustion treatment and sign the informed consent form.?Patients who are on mechanical ventilation >24h are eligible to participate in the study.?Eligible patients must have a diaphragm activity that measures under 20% and can be monitored through ultrasound.
Exclusion criteria
Exclusion criteria: 1.Patients who cannot receive acupuncture and moxibustion treatment due to pneumothorax, airway damage, local skin damage, or skin diseases are excluded from participation. 2.Patients with severe needle sickness or severe allergies are not eligible to participate. 3.Patients with life-threatening conditions such as circulatory, hematopoietic, or immune system diseases are excluded from participation. 4.Pregnant or lactating women are not eligible to participate. 5.Patients who are currently participating in other clinical trials are excluded from participation. 6.Lack of autonomous respiration.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| NICaS;The rear of interest for EIT;Variation rate of diaphragm thickness;diaphragmatic excursion (DE); | — |
Countries
China
Contacts
Public Contact???
The 2ed affiliated hospital of Harbin Medical University
Outcome results
None listed