An exploratory randomized controlled trial testing efficacy of adjunctive electrical muscle stimulation used in early rehabilitation in patients with sepsis
Not Applicable
- Conditions
- Sepsis
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Not provided
Exclusion Criteria
1.Presence of a pacemaker 2.Known primary systemic neuromuscular disease or intracranial disease at admission 3.Pre-hospitalization functional independence measure (FIM) score < 80, with inability to walk independently 4.Fracture or skin lesion (except contusion) in the region subjected to EMS (thigh, knee joint, ankle joint) 5.Pregnancy 6.Assessed as approaching or imminent death 7.Trauma 8.Unable to reach consensus 9.Determined by the physician-in-charge
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method