Status:
UNKNOWN
"Guarantee Assessment in Skin Prevention Adapted to Real Life With a Connected Device After a Spinal Cord Injury."
Lead Sponsor:
Nantes University Hospital
Conditions:
Spinal Cord Injury
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The investigators propose to test an embedded device on the seat of the wheelchair of paraplegic or tetraplegic patients (Gaspard), allowing on the one hand the continuous measurement of the pressures...
Eligibility Criteria
Inclusion
- Patients of both sexes with acquired spinal cord injury Traumatic or non-traumatic origin of the spinal cord injury
- Motor level \< C6
- Complete or incomplete injury (AIS A, B and C impairment scale)
- Primarily using a manual wheelchair (with or without electric propulsion assistance) as a means of mobility
- At least 18 years of age
- At any time after the occurrence of the spinal cord injury
- Patients discharged from the center, with a first post-injury rehabilitation completed
- Having participated in a specific therapeutic patient education on pressure ulcer prevention
- No pelvic pressure sores under medical or surgical treatment at the time of inclusion
- No aorto-iliac arterial disease that may promote pelvic ischemia (arterial Doppler \<6 months)
- Patient using a cushion approved by the HAS
- Patients with a smartphone
Exclusion
- Congenital spinal cord injury
- Motor level of the lesion \> or = C6
- Incomplete motor lesion (AIS D and E)
- Patients who walk as their primary mode of ambulation
- Use of an electric wheelchair
- Minors
Key Trial Info
Start Date :
June 1 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 1 2025
Estimated Enrollment :
242 Patients enrolled
Trial Details
Trial ID
NCT05403606
Start Date
June 1 2022
End Date
June 1 2025
Last Update
June 3 2022
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