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GET-UP Trial: Impact of an Early Out-of-bed Paradigm in Postoperative Outcomes of Chronic Subdural Hematomas

Impact of an Early Out-of-bed Paradigm in Postoperative Outcomes of Chronic Subdural Hematomas: GET-UP Randomized Prospective Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03788005
Acronym
GET-UP
Enrollment
208
Registered
2018-12-27
Start date
2019-04-07
Completion date
2022-08-05
Last updated
2021-08-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Subdural Hematoma

Keywords

Chronic Subdural Hematoma, Bed rest, Early mobilization

Brief summary

Compare rates of medical complications, recurrence and outcome in 2 randomized groups of patients with surgical chronic subdural hematomas. The intervention group will be assigned to early mobilization (within 12 hours of the surgical procedure). The control group will be assigned to bed rest for 48 hours.

Detailed description

At Centro Hospitalar do Porto it is routinely used burr hole craniostomy with subdural drains and 48 hours of bed rest for the surgical treatment of chronic subdural hematomas. After 48 hours the subdural drains are removed and the patient is allowed to mobilize for the first time. The aim of the present study is to conduct a prospective, randomized, controlled trial with an early mobilization protocol vs 48 hours bed rest to determine the best strategy to reduce postoperative complications and improve functional outcomes. There will be 2 groups: * Control group: bed rest 48 hours post-surgery with removal of subdural drains after this period. * Intervention group: Early mobilization protocol: as early mobilization as possible, within a maximum of 12 hours following surgery, with progressive autonomization in the ward as tolerated by the patient. Mobilization time will be recorded. At the time of assuming an upright position the drains will be closed and will only be open again when the patient is in supine position (8 hours per day of supine position). Subdural drains will be removed after 48 hours, similar to the practice in the control group. Primary End-Point: • Number of medical complications. Medical complication is defined as any occurrence which merits additional tests or, preferentially, requires any form of medical treatment. This includes respiratory infections, urinary infections, wound infections, meningitis, deep vein thrombosis, pulmonary embolism, cerebral infarction or hemorrhage, syncope, among others. Secondary End-Points: * Recurrence rates. A recurrence is defined as any chronic subdural hematoma ipsilateral to that of the original hematoma if a surgical strategy needs to be pursued. * Functional status (using both GOS-E and mRS). Timeframes considered will be pre-operative functional status, functional status at discharge, functional status at 3 months post-operative. * Mortality rates. * Recurrence free survival. * Time to discharge.

Interventions

PROCEDUREEarly mobilization

Early mobilization as soon as possible and within a maximum of 12 hours following burr hole craniostomy for chronic subdural hematomas.

Sponsors

Centro Hospitalar do Porto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Surgically drained chronic subdural hematomas (Burr hole craniostomy) * \> or equal to 18 years old

Exclusion criteria

* Previous neurosurgery * Surgery for another pathology performed at the same time * \> 6h sedation post-surgery * Any previous condition that makes early mobilization impossible

Design outcomes

Primary

MeasureTime frameDescription
Medical ComplicationsFrom date of randomization until 3 months post-randomizationInfections, venous thromboembolism, seizures

Secondary

MeasureTime frameDescription
RecurrenceAt 3 months follow-upRecurrence of a chronic subdural hematoma if surgical intervention is required
Post-operative Modified Rankin scaleAt 3 months follow-upModified Rankin Scale from 0 (free of symptoms) to a maximum of 6 (dead)
SurvivalAt 3 months follow-upSurvival
Length of hospital stayFrom date of randomization until clinical discharge up to 36 monthsTime to clinical discharge
Post-operative GOS-E scaleAt 3 months follow-upGOS-E scale from 1 (dead) to a maximum of 8 (upper good recovery - resumption of normal life within the capacity work even if pre-injury status has not been achieved; any existing deficits are not disabling)

Countries

Portugal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026