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

Primary Purpose

Chronic Subdural Hematoma

Status
Unknown status
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
Early mobilization
Sponsored by
Centro Hospitalar do Porto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Subdural Hematoma focused on measuring Chronic Subdural Hematoma, Bed rest, Early mobilization

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Centro Hospitalar Universitário do Porto

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Intervention group

Control Group

Arm Description

Early mobilization as soon as possible, within a maximum of 12 hours post-surgery. Subdural drains will be closed when the patient is allowed to mobilize and will be open during a nocturnal period of 8 hours. Subdural drains will be removed past 48 hours of surgery.

Bed rest with head of bed at 0 degrees for 48h. Subdural drains will be removed past 48 hours of surgery.

Outcomes

Primary Outcome Measures

Medical Complications
Infections, venous thromboembolism, seizures

Secondary Outcome Measures

Recurrence
Recurrence of a chronic subdural hematoma if surgical intervention is required
Post-operative Modified Rankin scale
Modified Rankin Scale from 0 (free of symptoms) to a maximum of 6 (dead)
Survival
Survival
Length of hospital stay
Time to clinical discharge
Post-operative GOS-E scale
GOS-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)

Full Information

First Posted
December 19, 2018
Last Updated
August 21, 2021
Sponsor
Centro Hospitalar do Porto
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1. Study Identification

Unique Protocol Identification Number
NCT03788005
Brief Title
GET-UP Trial: Impact of an Early Out-of-bed Paradigm in Postoperative Outcomes of Chronic Subdural Hematomas
Acronym
GET-UP
Official Title
Impact of an Early Out-of-bed Paradigm in Postoperative Outcomes of Chronic Subdural Hematomas: GET-UP Randomized Prospective Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
April 7, 2019 (Actual)
Primary Completion Date
August 5, 2021 (Actual)
Study Completion Date
August 5, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centro Hospitalar do Porto

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Subdural Hematoma
Keywords
Chronic Subdural Hematoma, Bed rest, Early mobilization

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
208 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Active Comparator
Arm Description
Early mobilization as soon as possible, within a maximum of 12 hours post-surgery. Subdural drains will be closed when the patient is allowed to mobilize and will be open during a nocturnal period of 8 hours. Subdural drains will be removed past 48 hours of surgery.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Bed rest with head of bed at 0 degrees for 48h. Subdural drains will be removed past 48 hours of surgery.
Intervention Type
Procedure
Intervention Name(s)
Early mobilization
Intervention Description
Early mobilization as soon as possible and within a maximum of 12 hours following burr hole craniostomy for chronic subdural hematomas.
Primary Outcome Measure Information:
Title
Medical Complications
Description
Infections, venous thromboembolism, seizures
Time Frame
From date of randomization until 3 months post-randomization
Secondary Outcome Measure Information:
Title
Recurrence
Description
Recurrence of a chronic subdural hematoma if surgical intervention is required
Time Frame
At 3 months follow-up
Title
Post-operative Modified Rankin scale
Description
Modified Rankin Scale from 0 (free of symptoms) to a maximum of 6 (dead)
Time Frame
At 3 months follow-up
Title
Survival
Description
Survival
Time Frame
At 3 months follow-up
Title
Length of hospital stay
Description
Time to clinical discharge
Time Frame
From date of randomization until clinical discharge up to 36 months
Title
Post-operative GOS-E scale
Description
GOS-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)
Time Frame
At 3 months follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sérgio Sousa, MD
Organizational Affiliation
Centro Hospitalar do Porto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centro Hospitalar Universitário do Porto
City
Porto
ZIP/Postal Code
4000
Country
Portugal

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
20336332
Citation
Kurabe S, Ozawa T, Watanabe T, Aiba T. Efficacy and safety of postoperative early mobilization for chronic subdural hematoma in elderly patients. Acta Neurochir (Wien). 2010 Jul;152(7):1171-4. doi: 10.1007/s00701-010-0627-4. Epub 2010 Mar 25.
Results Reference
background
PubMed Identifier
27834599
Citation
Brennan PM, Kolias AG, Joannides AJ, Shapey J, Marcus HJ, Gregson BA, Grover PJ, Hutchinson PJ, Coulter IC; British Neurosurgical Trainee Research Collaborative. The management and outcome for patients with chronic subdural hematoma: a prospective, multicenter, observational cohort study in the United Kingdom. J Neurosurg. 2017 Oct;127(4):732-739. doi: 10.3171/2016.8.JNS16134. Epub 2016 Nov 11.
Results Reference
background

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

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