Study of the Impact of the Use of a Corset on the Respiratory Function of Patients With Spinal Cord Injury
NCT ID: NCT01569360
Last Updated: 2013-12-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
PHASE3
INTERVENTIONAL
2012-03-31
2013-03-31
Brief Summary
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Detailed Description
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It is not known whether corset use discontinuation results from the spontaneous improvement respiratory function in the upright position or leads to the appearance of abdominal spasticity and to the improvement of respiratory function.
Therefore, we aim to study the effect of the long term corset use on SCI patients' respiratory function.
We will conduct a monocentric prospective open study of 56 SCI patients (SCI level ranging from C5 to T8 ASIA A or B) with a recent lesion (\<4 months). The evolution of respiratory function and dyspnea with and without corset use will be studied over a 2 years period. An evaluation of spasticity overtime will also be conducted. After randomization (corset use or not) evaluation will be conducted after 3 months, 6 months, 1 year and 2 years and will include: pulmonary function test with and without corset in the upright position and in the supine position, blood gases, dyspnea scores in the different positions and spasticity assessment.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Corset
the patients are assigned the use of a custome made corset during daytime
Corset
the patients are assigned the use of a custome made corset during daytime
No corset
the patients do not use a corset during daytime
No interventions assigned to this group
Interventions
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Corset
the patients are assigned the use of a custome made corset during daytime
Eligibility Criteria
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Inclusion Criteria
* Spinal cord injury with an ASIA score of A or B
* Spinal cord injury with an injury level from C5 to T8 (included)
* Initial injury \< 4 months
* Previous medical examination
* Signed consent form
Exclusion Criteria
* Refusal to participate to the study
* Pregnant or nursing women
* Previous corset use
* No affiliation to social security system
* Impossibility to sustain the sitting position for several weeks or months (due to skin sore or planned surgery …)
18 Years
ALL
No
Sponsors
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Assistance Publique - Hôpitaux de Paris
OTHER
Responsible Party
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Principal Investigators
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Helene Prigent, MD, PHD
Role: PRINCIPAL_INVESTIGATOR
Raymond Poincaré Hospital, Garches 92380 France
Other Identifiers
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P091121
Identifier Type: -
Identifier Source: org_study_id