Assessment of the Efficacy and Safety of EESS in Patients With Incomplete Spinal Cord Injuries
Recruiting
N/A
Interventional Study
Spinal Cord Injuries
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 65
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 14 (estimated)
- Sponsor
- Hopital Foch · Other
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About This Trial
Neurological disability caused by traumatic lesions of the spinal cord is a significant challenge for medicine and society. These lesions, leading to sublesional central nervous system dysfunction, include sensorimotor, vesico-sphincter and genito-sexual disorders. To date, there is no treatment that enables spinal cord function to be restored.
Preclinical studies have been able to demonstrate th…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Aged between 18 and 65 years inclusive
* Male or female
* Incomplete ASIA B or C spinal cord lesion with level of lesion located above T10 (sensation preserved below level of lesion)
* Absence of significant motor deficit of the upper limbs or recovered motor deficit (muscular…
Contacts