Mean Arterial Blood Pressure Treatment for Acute Spinal Cord Injury

Stopped early · Not applicable

Conditions studied: Acute Spinal Cord Injury

In brief

Current guidelines for the clinical management of acute spinal cord injury (SCI) recommend maintenance of mean arterial blood pressure (MAP) at 85 to 90 mmHg for the first seven days after SCI as a clinical option. Unfortunately, the medical evidence to support this recommendation exists only at the clinical case series level (Class III data). Furthermore, maintenance of sustained systemic hypertension, as per clinical guidelines, may be associated with risks to the patient via adverse medical events. Given this equivocal evidence, the investigators group has questioned the merit of sustained induced hypertension following acute SCI and has previously conducted a randomized, prospective controlled feasibility study to further examine this issue. This prior pilot study randomized patients with acute SCI to a spinal cord perfusion pressure (SCPP = MAP - intrathecal pressure (ITP)) target of ≥ 75 mmHg or to a control group (hypotension avoidance, MAP ≥ 65 mmHg). The primary endpoint measure was defined as the change in American Spinal Injury Association (ASIA) motor score from baseline. No difference in the primary outcome was noted at one-year post-SCI in this study. In light of this pilot data, the investigators hypothesize that maintenance of normotension (MAP ≥ 65mmHg) is not inferior to induced hypertension (MAP ≥ 85mmHg) for 7 days following acute SCI. As such, the investigators propose to conduct a Phase III non-inferiority prospective, randomized clinical trial in acute SCI patients. Subjects will be randomized into one of two MAP management groups for 7 days; Group 1 will be managed with a target MAP ≥ 65 mmHg, while Group 2 will be managed with a target MAP ≥ 85 mmHg. The primary endpoint will be change in ASIA motor score from baseline at 12 months post injury. A difference of ≤10 ASIA motor points change from baseline between groups will be considered as non-inferiority. Secondary endpoints will include ASIA sensory score, proportion of patients achieving a one grade improvement in ASIA impairment scale, quality of life assessment (as measured by Short-Form-36 \[SF-36\]) and functional outcome (as measured by the Spinal Cord Independence Measure (SCIM) and Functional Independence Measure (FIM). These will be measured at baseline, 72 hours and 3, 6 and 12 months from injury. Adverse events will be meticulously recorded. The information gleaned from this trial will provide valuable information for the acute treatment of traumatic SCI and will serve the objective of optimizing current clinical practice and thus maximizing medical and neurological outcome for individuals following acute traumatic SCI.

Key facts

Study ID

NCT02232165

Run by

University of Calgary

People needed

17

Starts

2013-02-01

Expected to finish

2019-09-20

Last updated by the study team

2019-09-25

Who can join

Age: 16 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age greater than or equal to 16 years.
• Motor complete or incomplete (ASIA A, B, or C) acute traumatic SCI involving spinal levels between C0 and T12.
• Written and informed consent from patient or a legally acceptable representative.
• Randomization and initiation of management protocol within 24 hours of injury.
• Reasonable expectation of availability to receive the full 7-day course of therapy and be available for follow up evaluations.

You may not qualify if…

• Acute traumatic SCI > 24 hours old.
• Central cord syndrome, defined as ASIA C or D with mean lower extremity score greater than upper extremity score.
• Isolated sensory deficit, motor intact.
• Isolated radicular motor deficit, defined as a unilateral motor deficit restricted to a single myotome.
• Pregnancy.
• Associated conditions interfering with informed consent or outcome assessment including closed head injury and major orthopedic injuries.
• Polytrauma: Abbreviated Injury Severity Score >3 in any area other than head.
• Known uncorrected severe coronary artery disease or evidence of active coronary ischemia (ECG changes, positive troponin) will be excluded.
• Advanced cardiac, pulmonary, hepatic or liver disease; the former will be operationally defined using NCI Toxicity Criteria (Grade 2 or higher).
• Allergy or other contraindication to norepinephrine.
• A known diagnosis of cancer (except basal cell cancer).
• Uncontrolled hypertension, defined as blood pressure persistently above 220 mmHg systolic or 120 mmHg diastolic, despite antihypertensive therapy.
• Any patients living in a nursing home or supervised living centre. Patients must be historically fully independent in all activities of daily living including banking, shopping, cooking, toileting, showering and dressing.
• Any other medical condition, in the investigator's opinion, for which the patient should not be included in the trial.
• Pre-existing and active major psychiatric or other chronic neurological disease.
• Patients who have a history of substance abuse or dependency within 12 months prior to the study.
• Currently participating in another interventional investigational study.

Where it is running

• University of Texas Health Science Center San Antonio — San Antonio, Texas, United States
• University of Calgary, Foothills Medical Centre — Calgary, Alberta, Canada

Full record on ClinicalTrials.gov

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