Applicability and Safety of Vibration Therapy in Intensive Care Unit (ICU) Patients (VTICU)
Status
Conditions
Treatments
Details and patient eligibility
About
Vibration therapy is used for different indications in rehabilitation and sports medicine. So far, vibration therapy has not been investigated within the ICU setting. The investigators created this setting to show safety and applicability of vibration therapy in ICU patients. 30 patients will be stimulated by vibration therapy on two separate days during their ICU stay. Three collectives of equal size will be observed: One with patients on mechanical ventilation without signs of infection or suspected intracranial pressure problems, a second one with patients on mechanical ventilation in addition to signs of systemic inflammation but absence of suspected intracranial pressure problems, and a third one with patients on mechanical ventilation, signs of systemic inflammation in addition to presence of controlled intracranial pressure problems. Typical parameters of hemodynamic status, intracranial pressure and energy metabolism will be recorded for a defined period of time before, during and after vibration therapy itself. Vibration therapy will be combined with protocol based physiotherapy.
Our aim is to show the effects of vibration therapy in ICU patients and its safe applicability.
ADDITION 06th of May 2011: Additionally we will perform euglycaemic hyperinsulinemic clamp and intervention on one day of ICU stay in 20 patients. Under clamp conditions we will perform a vibration therapy (ProMedVi Vibrosphere™) on patients' legs. On top we will perform electrical muscle stimulation (schwa-medico, MUSKELaktiv™) on one ventral upper leg, randomized chosen. Measuring the local skeletal muscle metabolism will be done by microdialysis in Vastus lateralis on both sides - comparing vibration therapy and vibration therapy combined with electrical muscle stimulation.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
-
immobilized icu patients:
- with mechanical ventilation without signs of infection
- with mechanical ventilation and SIRS or sepsis
- with mechanical ventilation, with controlled elevated intracranial pressure and with or without SIRS or sepsis
-
signed declaration of consent by the patient or its legal proxy
Exclusion criteria
- age < 18 years old
- already known neuromuscular disease
- missing declaration of consent by the patient or its legal proxy
- implanted heart pacemaker or defibrillator
- pregnancy
- acute thrombosis
- not yet healed fracture ad the part of the body which will be trained
- implants ad the part of the body which will be trained
- a nearly done ophthalmic surgery
- acute disc prolapse
- infaust prognosis, that means death is expected into the next couple of hours, although maximum therapy is done
Trial design
Primary purpose
Allocation
Interventional model
Masking
20 participants in 1 patient group
Trial contacts and locations
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal