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Accrual too slow; Study P.I. passed away.
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Chronic subdural hematoma (cSDH) is condition where blood has slowly leaked out of small blood vessels surrounding the brain. Over time, the blood may cause a variety of symptoms including headache, confusion, limb weakness, and difficulty speaking.
There is currently no agreement among physicians as to the best way to treat this condition.
The study hypothesis to be tested was: For patients with unilateral, symptomatic chronic subdural hematoma, there is no difference in clinical outcomes, as measured by achievement of modified Rankin Score of 0-2 at 6 months, between those treated with a 2 week course of oral dexamethasone, compared with those treated with burr hole surgical drainage.
Chronic subdural hematoma (cSDH) is condition where blood has slowly leaked out of small blood vessels surrounding the brain. Over time, the blood may cause a variety of symptoms including headache, confusion, limb weakness, and difficulty speaking.
There is currently no agreement among physicians as to the best way to treat this condition. One option is to do a surgery to drain the blood that has collected. Usually the surgery involves drilling small holes in the skull to relieve pressure and allow blood and fluids to be drained. Another option is to give medications such as steroids that might reduce the swelling. However, no drugs have been approved by the Food and Drug Administration (FDA) specifically to treat this condition. Some patients elect to have no treatment.
The purpose of this study was to investigate whether investigational treatment with a 2 week course of oral dexamethasone is as effective as surgery for cSDH. The study hypothesis to be tested was: For patients with unilateral, symptomatic chronic subdural hematoma, there is no difference in clinical outcomes, as measured by achievement of modified Rankin Score of 0-2 at 6 months, between those treated with a 2 week course of oral dexamethasone, compared with those treated with burr hole surgical drainage.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Burr Hole Craniostomy randomized | Active Comparator | Group receiving burr hole craniostomy and drainage of chronic subdural hematoma |
|
| Dexamethasone randomized | Experimental | Dexamethasone, tablet, initial dose 4mg q8h, total duration 15 days |
|
| Burr hole craniostomy observational | Other | Observational cohort of patients selecting burr hole craniostomy |
|
| Dexamethasone observational | Other | Observational cohort of patients treated with dexamethasone protocol |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Dexamethasone | Drug | Treatment with a short course of oral dexamethasone |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants With a Modified Rankin Score of 0, 1 or 2 | The Modified Rankin Scale (mRS) The mRS is evaluated as follows: 0 - No symptoms
Higher scores on the mRS scale mean a worse outcome. | 6 months after diagnosis |
| Measure | Description | Time Frame |
|---|---|---|
| Rate of Treatment Failure | This measure includes rate of repeat surgery in the burr hole group and rate of progression to surgery in the dexamethasone group | 6 months after diagnosis |
| Participants With Modified Rankin Score 0, 1 or 2 at 6 Months |
| Measure | Description | Time Frame |
|---|---|---|
| Rate of Radiographic Resolution of Chronic Subdural Hematoma | The data were not collected. | 6 months after diagnosis |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jennifer De Jong | University of Virginia | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Virginia Health System | Charlottesville | Virginia | 22908 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | Burr Hole Craniostomy Randomized | Group receiving burr hole craniostomy and drainage of chronic subdural hematoma Burr Hole Craniostomy |
| FG001 | Dexamethasone Randomized | Dexamethasone, tablet, initial dose 4mg q8h, total duration 15 days Dexamethasone |
| FG002 | Burr Hole Craniostomy Observational | Observational cohort of patients selecting burr hole craniostomy Burr Hole Craniostomy |
| FG003 | Dexamethasone Observational | Observational cohort of patients treated with dexamethasone protocol Dexamethasone |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
Population represents patients meeting inclusion/exclusion criteria who were enrolled in the study.
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| ID | Title | Description |
|---|---|---|
| BG000 | Burr Hole Craniostomy Randomized | Group receiving burr hole craniostomy and drainage of chronic subdural hematoma Burr Hole Craniostomy |
| BG001 | Dexamethasone Randomized | Dexamethasone, tablet, initial dose 4mg q8h, total duration 15 days Dexamethasone |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Number of Participants With a Modified Rankin Score of 0, 1 or 2 | The Modified Rankin Scale (mRS) The mRS is evaluated as follows: 0 - No symptoms
Higher scores on the mRS scale mean a worse outcome. | Number of Participants with a modified Rankin Score of 0, 1 or 2. | Posted | Count of Participants | Participants | 6 months after diagnosis |
|
6 months
Adverse events assessed included number of participants experiencing infection, seizure, medication intolerance, DVT and PE.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Burr Hole Craniostomy Randomized | Group receiving burr hole craniostomy and drainage of chronic subdural hematoma Burr Hole Craniostomy |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Daniel Raper | Department of Neurosurgery, University of Virginia Health System | 4349823244 | raper@virginia.edu |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Oct 20, 2015 | Aug 17, 2018 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D020200 | Hematoma, Subdural, Chronic |
| ID | Term |
|---|---|
| D006408 | Hematoma, Subdural |
| D020198 | Intracranial Hemorrhage, Traumatic |
| D020300 | Intracranial Hemorrhages |
| D002561 | Cerebrovascular Disorders |
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| ID | Term |
|---|---|
| D003907 | Dexamethasone |
| ID | Term |
|---|---|
| D011246 | Pregnadienetriols |
| D011245 | Pregnadienes |
| D011278 | Pregnanes |
| D013256 | Steroids |
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| Burr Hole Craniostomy | Procedure | Treatment with surgical burr hole craniostomy and evacuation of SDH |
|
|
The Modified Rankin Scale (mRS)
The mRS is evaluated as follows:
0 - No symptoms
Higher scores on the mRS scale mean a worse outcome.
| 6 months after hospital discharge |
| Participants With a Glasgow Coma Scale Score of 15 at 6 Month Follow-up | Glasgow Coma Scale (GCS) The GCS is evaluated on a scale from 3 to 15, with higher scores indicating better outcome. | 6 months after hospital discharge |
| Participants With a Markwalder Grading Score of 0 | Markwalder Grading Score (MGS) The MGS is assessed as follows: Grade 0 - Patient neurologically normal Grade 1 - Patient alert and oriented; mild symptoms, such as headache; absent or mild symptoms or neurologic deficit, such as reflex asymmetry Grade 2 - Patient drowsy or disoriented with variable neurological deficit, such as hemiparesis Grade 3 - Patient stuporous but responding appropriately to noxious stimuli; several focal signs, such as hemiparesis Grade 4 - Patient comatose with absent motor response to painful stimuli; decerebrate or decorticate posturing. Higher scores mean a worse outcome. | 6 months after hospital discharge |
| BG002 | Burr Hole Craniostomy Observational | Observational cohort of patients selecting burr hole craniostomy Burr Hole Craniostomy |
| BG003 | Dexamethasone Observational | Observational cohort of patients treated with dexamethasone protocol Dexamethasone |
| BG004 | Total | Total of all reporting groups |
| Participants |
|
| Age, Continuous | Mean | Full Range | years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race and Ethnicity Not Collected | Race and Ethnicity were not collected from any participant. | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
Group receiving burr hole craniostomy and drainage of chronic subdural hematoma
Burr Hole Craniostomy
| OG001 | Dexamethasone Randomized | Dexamethasone, tablet, initial dose 4mg q8h, total duration 15 days Dexamethasone |
| OG002 | Burr Hole Craniostomy Observational | Observational cohort of patients selecting burr hole craniostomy Burr Hole Craniostomy |
| OG003 | Dexamethasone Observational | Observational cohort of patients treated with dexamethasone protocol Dexamethasone |
|
|
| Secondary | Rate of Treatment Failure | This measure includes rate of repeat surgery in the burr hole group and rate of progression to surgery in the dexamethasone group | Reflects population analyzed for treatment failure. The one patient in the dexamethasone randomized group who died was not analyzed for this secondary outcome. | Posted | Count of Participants | Participants | 6 months after diagnosis |
|
|
|
| Secondary | Participants With Modified Rankin Score 0, 1 or 2 at 6 Months | The Modified Rankin Scale (mRS) The mRS is evaluated as follows: 0 - No symptoms
Higher scores on the mRS scale mean a worse outcome. | Posted | Count of Participants | Participants | 6 months after hospital discharge |
|
|
|
| Secondary | Participants With a Glasgow Coma Scale Score of 15 at 6 Month Follow-up | Glasgow Coma Scale (GCS) The GCS is evaluated on a scale from 3 to 15, with higher scores indicating better outcome. | Posted | Count of Participants | Participants | 6 months after hospital discharge |
|
|
|
| Secondary | Participants With a Markwalder Grading Score of 0 | Markwalder Grading Score (MGS) The MGS is assessed as follows: Grade 0 - Patient neurologically normal Grade 1 - Patient alert and oriented; mild symptoms, such as headache; absent or mild symptoms or neurologic deficit, such as reflex asymmetry Grade 2 - Patient drowsy or disoriented with variable neurological deficit, such as hemiparesis Grade 3 - Patient stuporous but responding appropriately to noxious stimuli; several focal signs, such as hemiparesis Grade 4 - Patient comatose with absent motor response to painful stimuli; decerebrate or decorticate posturing. Higher scores mean a worse outcome. | Posted | Count of Participants | Participants | 6 months after hospital discharge |
|
|
|
| Other Pre-specified | Rate of Radiographic Resolution of Chronic Subdural Hematoma | The data were not collected. | Not Posted | 6 months after diagnosis | Participants |
| 0 |
| 3 |
| 0 |
| 3 |
| 0 |
| 3 |
| EG001 | Dexamethasone Randomized | Dexamethasone, tablet, initial dose 4mg q8h, total duration 15 days Dexamethasone | 1 | 5 | 0 | 5 | 0 | 5 |
| EG002 | Burr Hole Craniostomy Observational | Observational cohort of patients selecting burr hole craniostomy Burr Hole Craniostomy | 0 | 1 | 0 | 1 | 0 | 1 |
| EG003 | Dexamethasone Observational | Observational cohort of patients treated with dexamethasone protocol Dexamethasone | 0 | 1 | 0 | 1 | 0 | 1 |
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| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D006259 | Craniocerebral Trauma |
| D020196 | Trauma, Nervous System |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D006406 | Hematoma |
| D006470 | Hemorrhage |
| D014947 | Wounds and Injuries |
| D000072473 |
| Fused-Ring Compounds |
| D011083 | Polycyclic Compounds |
| D013259 | Steroids, Fluorinated |
| Between 18 and 65 years |
|
| >=65 years |
|
| Male |
|