Respiratory Monitoring of Intrathecal Baclofen- a Feasibility Study
NCT03151941 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 15
Last updated 2017-10-10
Summary
The methodology is a feasibility study to determine the feasibility of assessing people in the community with a neurological condition before proceeding towards a full powered community trial evaluating the influence of intrathecal baclofen.
Conditions
- Intrathecal Baclofen
- Multiple Sclerosis
- Respiratory System
- Cerebral Palsy
Sponsors & Collaborators
-
Solent NHS Trust
lead OTHER_GOV
Principal Investigators
-
Hayden Kirk · Solent NHS Trust
Eligibility
- Min Age
- 18 Years
- Max Age
- 110 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-03-06
- Primary Completion
- 2017-08-31
- Completion
- 2017-08-31
Countries
- United Kingdom
Study Locations
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