Chronic Subdural Hematoma Clinical Trial
Official title:
Efficacy and Safety of Dexamethasone in Management of Chronic Subdural Hematoma: A Single Center Randomized Control Trial
Chronic subdural hematoma (cSDH) is a collection of blood and its breakdown products in the
subdural compartment. It is a condition frequently seen in any neurosurgical practice. cSDH
is believed to arise from tearing of bridging veins as a result of trauma, which may be minor
and unapparent to the patient. Management of cSDH is widely varied. A "wait-and-see" or
"wait-and-rescan" approach may be acceptable in asymptomatic patients with a relatively small
hematoma whilst cSDH with severe neurological deficits or decreased level of consciousness
may require surgical decompression by burr-hole craniostomy, twist drill craniostomy or
craniotomy. Surgery is associated with serious morbidity and mortality of up to 17% and
recurrence rates of 4%-33% requiring further treatment in some instances.The safety and
efficacy of different neurosurgical procedures have been evaluated but there is a paucity of
well-designed randomized controlled trials in the literature. Consequently, there is no
consensus on the best treatment with respect to surgical technique, pre-operative and
post-operative management and nonsurgical alternatives including the use of Corticosteroids,
Tranexamic acid, Osmotic diuretics, Atorvastatin or Angiotensin converting enzyme (ACE)
inhibitors.
Corticosteroids may be a therapeutic option in the management of cSDH. There is very little
data on the efficacy of corticosteroids in the treatment of cSDH and certainly no randomized
trials. The purpose of the study is to prove dexamethasone can be just as efficacious as
surgery in treating chronic subdural hematoma. The investigators also hope to show that those
patients treated with dexamethasone suffer less complication compared to those who undergo
surgery.
Status | Recruiting |
Enrollment | 326 |
Est. completion date | September 2021 |
Est. primary completion date | September 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - age = 18 yrs - subacute/chronic subdural hematoma on CT or MRI performed within 72 hours prior to recruitment - patient must be symptomatic Exclusion Criteria: - Glasgow Coma Scale (GCS) = 12 - patients needing craniotomy at the discretion of the on call neurosurgeon - hemiparesis with less than antigravity (= 3/5 medical research council scale) strength in any testable myotomes °= 2 seizures at presentation or history of epilepsy - subdural hematoma with an underlying lesion or condition such as tumor, arachnoid cyst, presence of a ventriculoperitoneal shunt or vascular malformation - contraindication to dexamethasone including allergy or hypersensitivity to dexamethasone, immunocompromised/immunosuppressed patients, uncontrolled diabetes, untreated known peptic ulcer disease - pregnant/breastfeeding mothers - acute infection including latent/active tuberculosis (TB) - history of psychosis - anticoagulated for mechanical heart valve or arterial stent (i.e. coronary, carotid, or peripheral) placement - small volume, non-operable subdural collection |
Country | Name | City | State |
---|---|---|---|
Canada | University of Calgary | Calgary | Alberta |
Lead Sponsor | Collaborator |
---|---|
University of Calgary |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Failure rates | Failure is defined as the requirement for surgical intervention in the dexamethasone group or re-operation in the surgical group. | 3 months | |
Secondary | Recurrence rate | Recurrence is defined as symptomatic and radiologic re-accumulation of subdural hematoma on the ipsilateral side requiring a reoperation within 3months after treatment. | 3 months | |
Secondary | Modified Ranking Scale | Functional outcome | 1, 3 and 6 months after treatment | |
Secondary | Barthel index | Functional outcome | 1, 3 and 6 months after treatment | |
Secondary | Glasgow Outcome Scale | Functional outcome | 1, 3 and 6 months after treatment | |
Secondary | Glasgow Coma Scale | Functional outcome | 1, 3 and 6 months after treatment | |
Secondary | Markwalder score | Functional outcome | 1, 3 and 6 months after treatment | |
Secondary | Clinical improvement (Categorized as resolved, improved, unchanged or worse) | Categorized as resolved, improved, unchanged or worse | 1, 3 and 6 months after treatment | |
Secondary | Radiologic outcomes (Change in hematoma volume) | Measured as change in hematoma volume | 1, 3 and 6 months after treatment | |
Secondary | Quality of Life measured using the EQ-5D-5L | Quality of life will be measured using the EuroQol health survey (EQ-5D-5L) questionnaire. | 1, 3 and 6 months after treatment | |
Secondary | Mortality | 1, 3 and 6 months |
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