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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02786966
Other study ID # CTO 0769
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2017
Est. completion date May 31, 2018

Study information

Verified date September 2018
Source Ottawa Hospital Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Each year, half a million patients with a potential neck (c-spine) injury are transported to Ontario emergency departments (ED). Less than 1% of all these patients actually have a neck bone fracture. Even less (0.5%) have a spinal cord injury or nerve damage. These injuries usually occur at the time of initial trauma and not during transport to the ED. Currently, paramedics transport all trauma victims (with or without an injury) by ambulance using a backboard, collar, and head immobilizers. Trauma victims can stay immobilized for hours until an ED bed is made available or until x-rays are completed. Importantly, long immobilization is often unnecessary, it causes patient discomfort and pain, decreases community access to paramedics, contributes to ED crowding, and is very costly.

The investigators developed the Canadian C-Spine Rule (CCR) for alert and stable trauma patients. This decision rule helps ED physicians and triage nurses to safely and selectively remove immobilization, without x-rays and missed injury.

The investigators will evaluate the possibility and benefits of allowing paramedics to use the CCR in the field in 12 new communities from across Ontario. Patients have suggested the investigators include measures of pain and discomfort from being immobilized during transport as important patient-centred outcomes. The investigators will also measure the impact on the ED, and how much money could be saved if more paramedics were allowed to use the CCR. The investigators will also assess if sex, age, language barriers, or living far from the hospital (long transport time) will affect the outcomes of the study.


Description:

Paramedics in participating Ontario communities will all receive standardized training on the application of the Canadian C-Spine Rule (CCR). Once the training has been completed, paramedics will begin using the CCR to evaluate patients with potential c-spine injuries. For the first three months of the evaluation period, paramedics will use the CCR to evaluate eligible patients, but continue to use spinal immobilization for transport according to their existing protocols. After this validation period, participating services will be randomized in stepped wedge fashion in clusters of 4 services to actively use the CCR and selectively immobilize according to the CCR.


Recruitment information / eligibility

Status Completed
Enrollment 6560
Est. completion date May 31, 2018
Est. primary completion date April 30, 2018
Accepts healthy volunteers No
Gender All
Age group 8 Years and older
Eligibility Inclusion Criteria:

- Alert (Glasgow Coma Scale 15)

- Stable: Adult (16+): systolic blood pressure greater than or equal to 90 mmHg, respiratory rate 10-24 breaths/minute; Child (8-15): systolic blood pressure greater than or equal to 90 mmHg + (2 X age in years), respiratory rate 14-20 breaths/minute

- Acute blunt injury (within 48 hours of paramedic contact)

Exclusion Criteria:

- Age <8 years of age

- Penetrating trauma from stabbing or gunshot wound

- Acute paralysis (paraplegia, quadriplegia)

- Known vertebral disease (ankylosing spondylitis, rheumatoid arthritis, spinal stenosis, previous c-spine surgery)

- Referred from another hospital

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Canadian C-Spine Rule
Paramedic assessment for potential cervical spine injuries using the Canadian C-Spine Rule

Locations

Country Name City State
Canada Ottawa Hospital Research Institute Ottawa Ontario

Sponsors (2)

Lead Sponsor Collaborator
Ottawa Hospital Research Institute The Ontario Spor Support Unit

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Proportion of patients with a pain score </= 4/10 through study completion (one year)
Other Time from paramedic arrival at patient side to ED discharge or admission to hospital through study completion (one year)
Other Radiation Exposure radiation exposure from diagnostic imaging tests of the spine conducted at initial visit or within 30 days of the initial visit through study completion (one year)
Other Number of skin pressure injuries through study completion (one year)
Other Number of missed cervical spine injuries through study completion (one year)
Other Paramedic Field Time (arrival at patient side until departure for hospital) arrival at patient side until departure for hospital through study completion (one year)
Other Paramedic Hospital Time from arrival at emergency department to transfer of care to emergency department staff through study completion (one year)
Other Subsequent emergency department visits or hospital admissions within 30 days of initial visit through study completion (one year)
Other Subsequent clinic or family physician visits within 30 days of initial visit through study completion (one year)
Other Frequency of Cervical Spine diagnostic imaging at initial visit or within 30 days of initial visit through study completion (one year)
Other Cost Savings incremental cost saving per one immobilization avoided through study completion (one year)
Primary Proportion of patients transported with spinal immobilization through study completion (one year)
Primary Proportion of patients feeling comfortable through study completion (one year)
See also
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