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Clinical Trials/ISRCTN91943864
ISRCTN91943864
Completed
未知

A feasibility study investigating different interventions for the treatment of benign paroxysmal positional vertigo in acute traumatic brain injury patients

Imperial College London0 sites75 target enrollmentFebruary 13, 2020
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Imperial College London
Enrollment
75
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

2020 Protocol article in https://pubmed.ncbi.nlm.nih.gov/32944278/ protocol (added 21/09/2020) 2023 Interim results article in https://pubmed.ncbi.nlm.nih.gov/36592999/ Qualitative results on healthcare professionals' perceptions of barriers or facilitators (added 03/01/2023) 2024 Results article in https://doi.org/10.1136/bmjno-2023-000598 (added 31/05/2024)

Registry
who.int
Start Date
February 13, 2020
End Date
April 1, 2022
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1\. Over the age of 18 years
  • •2\. Closed head injury as defined by CT imaging
  • •3\. Inpatient on major trauma or outlying ward
  • •4\. Able to give informed consent or consultee consent
  • •5\. Sufficient grasp of English to consent and complete outcome measures
  • •Staff inclusion criteria:
  • •1\. Members of ward staff involved in the trial
  • •2\. Able to consent to an audio\-recorded interview

Exclusion Criteria

  • •Patients exclusion criteria:
  • •1\. History of previous or current substance abuse
  • •2\. Orthopaedic or vascular cervical spine instability
  • •3\. Pregnant
  • •4\.Glasgow Coma Score at assessment less than 14
  • •5\. Medically unstable
  • •6\. Current prescription of Phenytoin
  • •7\. Active psychiatric disease, including those with a current or past history of active psychotic disease but not those with a past history of psychiatric disease
  • •Staff exclusion criteria:
  • •Does not meet inclusion criteria

Outcomes

Primary Outcomes

Not specified

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