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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03526211
Other study ID # 18CH005
Secondary ID 2018-A00541-54
Status Completed
Phase N/A
First received
Last updated
Start date July 24, 2018
Est. completion date June 18, 2019

Study information

Verified date June 2019
Source Centre Hospitalier Universitaire de Saint Etienne
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Intensive care unit acquired muscle weakness (ICUAW), is a common disease which influence rehabilitation, extend mechanical ventilation and length of stay in intensive care unit, and affect quality of life at hospital discharge.

To prevent ICUAW, different strategies of early mobilization are recommended. But all cannot be applied in all ICU patients. Some of them benefit from heavy therapies like circulatory assistance or renal replacement therapy for example, that limit mobilization.

Cycloergometer is a tool that allows continuous passive mobilization in bedridden and even unconscious patients.

Neuromuscular electrical stimulation (NMES) is an alternative that helps preserve muscle mass and limit muscle atrophy.

Early bedside cycle exercise coupled with NMES is an interesting new approach where application of an electrical stimulation along specific motor nerves on each lower limb, generates muscles contractions and pedaling on cycloergometer.

The aim of this study is to evaluate safety and feasibility of this coupled technique called Functional Electrical Stimulation (FES) Cycling, in ICU patients.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 18, 2019
Est. primary completion date June 18, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age = 18 years

- Deeply sedated (Riker 1-2) patients, admitted in intensive care unit B of ST-Etienne hospital

- Without curare since 12 hours

- Normothermic or with a controlled fever (central temperature between 36 and 38°C)

- Without haemodynamic instability (mean arterial pressure > 65mmHg and < 120mmHg, systolic arterial pressure > 90mmHg and < 200mmHg, Norepinephrine < 4mg/h)

- Without respiratory instability (respiratory rate < 35/min, pulse oxymetry > 90%, inspired oxygen fraction < 60%, PaO2/FiO2 ratio > 250, Peep < 10cmH2O, with invasive mechanical ventilation)

- Without neurological instability (diastolic velocities in mean cerebral artery > 30cm/s, mean velocities > 50cm/s, pulsatility index < 1.2, intracranial pressure < 20mmhg, brain tissue oxygenation tension > 15mmHg)

- Patient whose family has given informed and written consent to the patient's participation in the study

Exclusion Criteria:

- Pregnant woman,

- Patients with peripheral nerve damage prior to or at the time of measurement

- Curarized patients (non-efficacy of neurostimulation)

- Presence of a catheter in the stimulation zone (femoral artery or vein)

- Patients with lower limb, pelvic or spine fracture

- Patients with continuous renal replacement therapy

- Patients with circulatory assistance

- Patients with wounds in electrodes placement area

- Morbidly obesity with Ideal Body Weight > 40kg/m2

- Patients with pacemaker

- Lower limb deep vein thrombosis without treatment

Study Design


Related Conditions & MeSH terms


Intervention

Device:
FES cycling
On the patient, three pairs of electrodes will be applied on tibial hamstring, quadriceps and gluteal muscles of each lower limb. Cycloergometer will be installed in passive mode. Then, optimal stimulation intensity for each muscle will be defined. During twenty minutes, neuromuscular electrical stimulation will generate a passive pedaling on cycloergometer.

Locations

Country Name City State
France Chu Saint-Etienne Saint-Étienne

Sponsors (2)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Saint Etienne Laboratoire de Physique ENS de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Tolerance Number of FES Cycling sessions that must be stopped because of the presence of at least 1 following criteria (these criteria are qualitative (presence or absence) and therefore do not add up):
Mean arterial pressure <65mmHg or> 120mmHg,
Systolic blood pressure <90 mmHg or> 200 mmHg,
Heart rate <50 or> 130 / min
Occurrence of atrial or ventricular arrhythmia
Respiratory rate > 35 / min,
Pulse oxygen saturation <90%
Intracranial pressure > 20mmHg.
Mean mean arterial velocity measured by transcranial Doppler <30 cm / s
During the FES Cycling session (day 1)
Secondary Systolic blood pressure Haemodynamic repercussions of a FES Cycling session measured by Systolic blood pressure During the FES Cycling session (day 1)
Secondary Haemodynamic tolerance Heart rate Haemodynamic repercussions of a FES Cycling session measured by Heart rate During the FES Cycling session (day 1)
Secondary Cardiac output measured Haemodynamic repercussions of a FES Cycling session measured by Cardiac output measured in transthoracic echocardiography During the FES Cycling session (day 1)
Secondary Fick equation Haemodynamic repercussions of a FES Cycling session measured by oxygen consumption according to the Fick equation (cardiac output x (arterial content in O2 - venous content in O2)) During the FES Cycling session (day 1)
Secondary Arterial lactates Haemodynamic repercussions of a FES Cycling session measured Arterial lactates During the FES Cycling session (day 1)
Secondary Venous oxygen Haemodynamic repercussions of a FES Cycling session measured by Venous oxygen saturation During the FES Cycling session (day 1)
Secondary Amine dosage Haemodynamic repercussions of a FES Cycling session measured by Amine dosage During the FES Cycling session (day 1)
Secondary Respiratory tolerance Oxygen saturation Respiratory repercussions of a FES Cycling session measured by Oxygen saturation During the FES Cycling session (day 1)
Secondary Respiratory tolerance Respiratory repercussions of a FES Cycling session measured by Respiratory rate During the FES Cycling session (day 1)
Secondary Respiratory rate Respiratory repercussions of a FES Cycling session measured by PaCO2 and PaO2 During the FES Cycling session (day 1)
Secondary Diastolic cerebral artery Neurological repercussions of a FES Cycling session measured by diastolic average cerebral artery measured by transcranial Doppler During the FES Cycling session (day 1)
Secondary Pulsatility index Neurological repercussions of a FES Cycling session measured by Average of pulsatility index, measured by transcranial Doppler. During the FES Cycling session (day 1)
Secondary Intracranial pression Neurological repercussions of a FES Cycling session measured by, If sensors present, Intracranial pression. During the FES Cycling session (day 1)
Secondary Cerebral perfusion pressure Neurological repercussions of a FES Cycling session measured by, If sensors present, Cerebral perfusion pressure. During the FES Cycling session (day 1)
Secondary Cerebral tissue oxygen pressure Neurological repercussions of a FES Cycling session measured by, If sensors present, Cerebral tissue oxygen pressure. During the FES Cycling session (day 1)
Secondary FES cycling installation FES Cycling technical feasibility measured by installation and uninstallation times Cycloergometer, After the FES Cycling session (day 1)
Secondary FES Cycling technical feasibility FES Cycling technical feasibility measured by number of persons needed. After the FES Cycling session (day 1)
Secondary Duration of FES Cycling session FES Cycling technical feasibility measured by total duration of FES Cycling session. After the FES Cycling session (day 1)
Secondary Failure FES Cycling session FES Cycling technical feasibility measured by number of procedural failures. After the FES Cycling session (day 1)
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