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
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UNKNOWN
NA
50 participants
INTERVENTIONAL
2020-10-01
2021-10-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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experimental group
Early standing training and routine rehabilitation
Intensive rehabilitation
Early standing training and routine rehabilitation
control group
Conventional rehabilitation,Muscle training and breathing training
Intensive rehabilitation
Early standing training and routine rehabilitation
Interventions
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Intensive rehabilitation
Early standing training and routine rehabilitation
Eligibility Criteria
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Inclusion Criteria
* the hemodynamics is stable;
* 50 \< heart rate \< 120 beats / min ;
* 90 \< systolic blood pressure \< 200mmHg ;
* 55 \< mean arterial pressure \< 120mmHg;
* do not increase the dose of pressor drugs for at least 2 hours;
* intracranial pressure is stable and there are no seizures within 24 hours;
* the respiratory state is stable;
* the patient's finger pulse oxygen saturation ≥ 88%;
* Oxygen concentration less than 60%;
* Terminal positive expiratory pressure\<12cmH2O;
* 10 \< respiratory frequency \< 35 beats / min.
Exclusion Criteria
* acute cardio-cerebrovascular events;
* spinal or limb fractures;
* active bleeding.
18 Years
100 Years
ALL
No
Sponsors
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Chinese PLA General Hospital
OTHER
Responsible Party
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wang kaifei
Ph.D.
Principal Investigators
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xin li xie
Role: PRINCIPAL_INVESTIGATOR
The First Medical Center of PLA General Hospital
Central Contacts
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Other Identifiers
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Intensive rehabilitation
Identifier Type: -
Identifier Source: org_study_id
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