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Evaluation of Surgery in Elderly With Traumatic Acute SubDural Hematoma (RESET-ASDH)

Primary Purpose

Intracranial Hemorrhages, Surgery

Status
Withdrawn
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Early neurosurgical hematoma evacuation
Conservative treatment (best medical management)
Sponsored by
Leiden University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Intracranial Hemorrhages focused on measuring Neurosurgery, Acute subdural hematoma, Traumatic brain injury

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age ≥ 65 years
  • A GCS of ≥ 9 and a traumatic ASDH >10 mm in diameter or a traumatic ASDH <10 mm but with a midline shift >5 mm, or a GCS <9 and a traumatic ASDH <10 mm and a midline shift <5 mm without extracranial explanations for the comatose condition
  • Clinical equipoise exists (i.e. the responsible neurosurgeon is uncertain about the benefits of either treatment)
  • Informed consent is obtained or deferred

Exclusion Criteria:

  • Additional epidural hematoma (EDH) or infratentorial (e.g. cerebellar) intracerebral hemorrhage (ICH)
  • Major traumatic abdominal or thoracic injury (each separately defined as an Abbreviated Injury Scale (AIS) score ≥ 4) or a 'moribund' state at presentation (e.g. bilaterally absent pupillary responses)
  • Known terminal condition resulting in a life expectancy of less than 1 year

Sites / Locations

  • Leiden University Medical Center (LUMC)

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Early surgery

Initial conservative treatment

Arm Description

Outcomes

Primary Outcome Measures

Glasgow Outcome Scale Extended (GOS-E)
scale of functional outcome ranging from 1-8 in which a higher score reflects a better recovery

Secondary Outcome Measures

Full Information

First Posted
November 16, 2020
Last Updated
June 22, 2023
Sponsor
Leiden University Medical Center
Collaborators
Haaglanden Medisch Centrum, Amsterdam Universitair Medisch Centrum, Erasmus Medical Center, Elisabeth-TweeSteden Ziekenhuis, Medisch Spectrum Twente, Radboud Universitair Medisch Centrum, Utrecht Universitair Medisch Centrum, Universitair Ziekenhuis Leuven, Algemeen Ziekenhuis Sint-Jan Brugge, Universite Libre de Bruxelles, Erasme Hospital Universite Libre de Bruxelles, University Hospital, Antwerp, Ziekenhuis Oost-Limburg, Centre Hospitalier Universitaire de Liege, Algemeen Ziekenhuis Delta, Funding agencies: ZonMw / KCE (BeNeFIT)
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1. Study Identification

Unique Protocol Identification Number
NCT04648436
Brief Title
Evaluation of Surgery in Elderly With Traumatic Acute SubDural Hematoma
Acronym
RESET-ASDH
Official Title
Survival and Quality of Life After Early Surgical Intervention Versus Wait-and-see in Elderly Patients With a Traumatic Acute Subdural Hematoma (ASDH): a Pragmatic Randomized Controlled Trial With Multicenter Parallel Group Design
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Withdrawn
Why Stopped
Lack of inclusion / COVID-19 regulations
Study Start Date
March 1, 2022 (Anticipated)
Primary Completion Date
March 23, 2023 (Actual)
Study Completion Date
March 23, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Leiden University Medical Center
Collaborators
Haaglanden Medisch Centrum, Amsterdam Universitair Medisch Centrum, Erasmus Medical Center, Elisabeth-TweeSteden Ziekenhuis, Medisch Spectrum Twente, Radboud Universitair Medisch Centrum, Utrecht Universitair Medisch Centrum, Universitair Ziekenhuis Leuven, Algemeen Ziekenhuis Sint-Jan Brugge, Universite Libre de Bruxelles, Erasme Hospital Universite Libre de Bruxelles, University Hospital, Antwerp, Ziekenhuis Oost-Limburg, Centre Hospitalier Universitaire de Liege, Algemeen Ziekenhuis Delta, Funding agencies: ZonMw / KCE (BeNeFIT)

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
Rationale: The rapidly increasing number of elderly (≥ 65 years old) with traumatic brain injury (TBI) is accompanied by substantial medical and economic consequences. An intracranial hematoma, specifically an acute subdural hematoma (ASDH), is the most common injury in elderly with TBI. The surgical versus conservative treatment of this patient group remains an important clinical and moral dilemma, since it is in most cases unclear which treatment leads to a better outcome for the patient. Current guidelines are not based on high-quality evidence and compliance is low, allowing for large treatment variation in both Belgium and the Netherlands for patients with a traumatic ASDH. In addition, elderly are underrepresented in scientific TBI literature and are therefore not included in current guidelines or prognostic models, leading to major uncertainty in (neurosurgical) decision-making for this group. As participants in two large TBI research projects (CENTER-TBI, Net-QuRe), the investigators observe that the uncertainty regarding treatment of elderly with a traumatic ASDH will not be solved by the current ongoing studies. Therefore, they recognize the necessity of undertaking a prospective, randomized, multicenter trial on the (cost-)effectiveness of early surgical hematoma evacuation versus a conservative treatment in elderly with a traumatic ASDH. Objective: To compare the (cost-)effectiveness of early surgical hematoma evacuation versus a conservative treatment in elderly patients with a traumatic ASDH. Study design: A prospective, pragmatic, multicenter, randomized controlled trial (RCT). Study population: Patients ≥ 65 years with at first presentation a GCS ≥ 9 and a traumatic ASDH >10 mm or a traumatic ASDH <10 mm and a midline shift >5 mm, or a GCS < 9 with a traumatic ASDH <10 mm and a midline shift <5 mm without extracranial explanations for the comatose state, for whom clinical equipoise exists regarding the preferred treatment. Intervention: Patients are randomized to either early surgical hematoma evacuation (A) or conservative management on the ICU or the ward (B). In case of neurological deterioration during conservative management, delayed surgery can be performed. The exact neurosurgical technique will be left to the discretion of the surgeons. Main study parameters/endpoints: Functional outcome after 1 year, expressed by the rating on the Extended Glasgow Outcome Scale (GOS-E) Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Both treatment strategies are already used in current clinical practice as standard medical care. Therefore, there are no extra risks for patients participating in the study compared to patients outside the study. Study participation adds a minimal burden of three follow-up evaluations by visit in the first year (at 3, 6 and 12 months) and subsequent yearly evaluations by phone or postal until five years after the injury. Future elderly patients with a traumatic ASDH will benefit mostly from this study's results.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intracranial Hemorrhages, Surgery
Keywords
Neurosurgery, Acute subdural hematoma, Traumatic brain injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial with parallel group design
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Early surgery
Arm Type
Other
Arm Title
Initial conservative treatment
Arm Type
Other
Intervention Type
Other
Intervention Name(s)
Early neurosurgical hematoma evacuation
Intervention Description
Early neurosurgical hematoma evacuation (preferably within 2 hours)
Intervention Type
Other
Intervention Name(s)
Conservative treatment (best medical management)
Intervention Description
Conservative treatment (best medical management) on the ICU or ward
Primary Outcome Measure Information:
Title
Glasgow Outcome Scale Extended (GOS-E)
Description
scale of functional outcome ranging from 1-8 in which a higher score reflects a better recovery
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age ≥ 65 years A GCS of ≥ 9 and a traumatic ASDH >10 mm in diameter or a traumatic ASDH <10 mm but with a midline shift >5 mm, or a GCS <9 and a traumatic ASDH <10 mm and a midline shift <5 mm without extracranial explanations for the comatose condition Clinical equipoise exists (i.e. the responsible neurosurgeon is uncertain about the benefits of either treatment) Informed consent is obtained or deferred Exclusion Criteria: Additional epidural hematoma (EDH) or infratentorial (e.g. cerebellar) intracerebral hemorrhage (ICH) Major traumatic abdominal or thoracic injury (each separately defined as an Abbreviated Injury Scale (AIS) score ≥ 4) or a 'moribund' state at presentation (e.g. bilaterally absent pupillary responses) Known terminal condition resulting in a life expectancy of less than 1 year
Facility Information:
Facility Name
Leiden University Medical Center (LUMC)
City
Leiden
State/Province
Zuid Holland
ZIP/Postal Code
2333ZA
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
35351178
Citation
Singh RD, van Dijck JTJM, van Essen TA, Lingsma HF, Polinder SS, Kompanje EJO, van Zwet EW, Steyerberg EW, de Ruiter GCW, Depreitere B, Peul WC. Randomized Evaluation of Surgery in Elderly with Traumatic Acute SubDural Hematoma (RESET-ASDH trial): study protocol for a pragmatic randomized controlled trial with multicenter parallel group design. Trials. 2022 Mar 29;23(1):242. doi: 10.1186/s13063-022-06184-1.
Results Reference
derived

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Evaluation of Surgery in Elderly With Traumatic Acute SubDural Hematoma

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