Respiratory Monitoring of Intrathecal Baclofen- a Feasibility Study

Status Completed

Clinical Trial 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.

Clinical Trial Description

The purpose of this proposed research will evaluate a feasible method to assess the respiratory status of people with neurological conditions receiving or scheduled to receive Intrathecal Baclofen. The use of Intrathecal Baclofen to manage severe spasticity is a developing treatment option with a limited research base, particularly when evaluating the influence of intrathecal baclofen on the respiratory system. The proposed research is derived from clinical practice and involves joint collaboration between clinical team, research professionals and patients.

In order for the study to evaluate the influence of Intrathecal baclofen has on the respiratory system, the proposed research will need to develop and evaluate a method of assessing people in the community ensuring it's feasible for people with neurological conditions. Prior to implementing a full powered community trial to evaluate the influence of intrathecal baclofen on people with neurological conditions. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03151941
Study type	Observational
Source	Solent NHS Trust
Contact
Status	Completed
Phase	N/A
Start date	March 6, 2017
Completion date	August 31, 2017

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