Respiratory Monitoring of Intrathecal Baclofen- a Feasibility Study

NCT03151941 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 15

Last updated 2017-10-10

No results posted yet for this study

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

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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03151941 on ClinicalTrials.gov