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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04592679
Other study ID # 3879B
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2015
Est. completion date July 21, 2020

Study information

Verified date October 2020
Source Azienda Ospedaliero, Universitaria Pisana
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

20 patients were recruited by two hospitals (AOUP and AOUC) in Italy from January 2015 to January 2018. The participants have been addressed to two different groups: the ones recruited by the AOUP were submitted to an experimental protocol of rehabilitation with FES Cycling, the ones recruited by the AOUC were submitted to a standard protocol of manual mobilization. The primary outcome was the thigh circumferences measured at 4 different levels (5-10-15-20 cm) from the superior margin of the patella, while the secondary outcomes were the muscle tone evaluated with Modified Ashworth Scale (MAS) and the sensation of pain registered with International Spinal Cord Injury - Pain Basic Data Set (ISCI-P). From these outcomes the Quality Adjusted Life Years (QALYs) was obtained. The costs of the two treatments were calculated through a consultation process with the Competent Offices of the two hospitals. The QALYs and the costs were used to calculate the Incremental Cost-Effectiveness Ratio (ICER) in order to verify the cost-effectiveness ratio of the two treatments.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date July 21, 2020
Est. primary completion date January 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - complete spinal cord injury - loss of gait function - any episode of autonomic dysreflexia - any important range of motion limitation to hips, knees or ankles - eccitability of the muscles - FES tollerability Exclusion Criteria: - cognitive deficits - psychiatric diseases - cancer - recent fractures

Study Design


Intervention

Device:
FES-C
The participants were submitted to 20 sessions of FES-C three/five times per week. Each session lasted about 30'.
Other:
Standard Treatment
The participants were submitted to 20 sessions of standard rehabilitation for lower limbs with manual mobilization, three/five times per week. Each session lasted about 30'.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Azienda Ospedaliero, Universitaria Pisana

Outcome

Type Measure Description Time frame Safety issue
Primary Incremental Cost-Effectiveness Ratio QALYs/costs of the two treatments, the ICER could variate from -100'000 to 100'000 QALYs/€ 3 years
Primary Thigh Circumferences The primary outcome was the thigh circumferences measured at 4 different levels (5-10-15-20 cm) from the superior margin of the patella, the raging of the improvement could be from 0 to 50 cm 3 years
Secondary Quality Adjusted Life Years (QALYs) It consists in the use of a scale 0 (death) - 1 (the best possible state of health) for the improvements of the patients 3 years
Secondary Costs the costs of the two treatments could variate from 0 to 50'000 € 3 years
Secondary Muscle tone Muscle tone evaluated with "Modified Ashworth Scale" (MAS), 0-5 points, an higher result means more spasticity 3 years
Secondary Sensation of pain Sensation of pain evaluated with "International Spinal Cord Injury - Pain Basic Data Set" 0-30 points, an higher result means more sensation of pain (ISCI-P). 3 years
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