Evaluation of Surgery in Elderly With Traumatic Acute SubDural Hematoma

NCT ID: NCT04648436

Last Updated: 2023-06-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2022-03-01

Study Completion Date

2023-03-23

Brief Summary

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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.

Detailed Description

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Conditions

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Intracranial Hemorrhages Surgery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomized controlled trial with parallel group design
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Early surgery

Group Type OTHER

Early neurosurgical hematoma evacuation

Intervention Type OTHER

Early neurosurgical hematoma evacuation (preferably within 2 hours)

Initial conservative treatment

Group Type OTHER

Conservative treatment (best medical management)

Intervention Type OTHER

Conservative treatment (best medical management) on the ICU or ward

Interventions

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Early neurosurgical hematoma evacuation

Early neurosurgical hematoma evacuation (preferably within 2 hours)

Intervention Type OTHER

Conservative treatment (best medical management)

Conservative treatment (best medical management) on the ICU or ward

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Haaglanden Medisch Centrum

UNKNOWN

Sponsor Role collaborator

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

OTHER

Sponsor Role collaborator

Erasmus Medical Center

OTHER

Sponsor Role collaborator

Elisabeth-TweeSteden Ziekenhuis

OTHER

Sponsor Role collaborator

Medisch Spectrum Twente

OTHER

Sponsor Role collaborator

Radboud Universitair Medisch Centrum

UNKNOWN

Sponsor Role collaborator

Utrecht Universitair Medisch Centrum

UNKNOWN

Sponsor Role collaborator

Universitair Ziekenhuis Leuven

UNKNOWN

Sponsor Role collaborator

Algemeen Ziekenhuis Sint-Jan Brugge

UNKNOWN

Sponsor Role collaborator

Universite Libre de Bruxelles

UNKNOWN

Sponsor Role collaborator

Erasme Hospital Universite Libre de Bruxelles

UNKNOWN

Sponsor Role collaborator

University Hospital, Antwerp

OTHER

Sponsor Role collaborator

Ziekenhuis Oost-Limburg

OTHER

Sponsor Role collaborator

Centre Hospitalier Universitaire de Liege

OTHER

Sponsor Role collaborator

Algemeen Ziekenhuis Delta

UNKNOWN

Sponsor Role collaborator

Funding agencies: ZonMw / KCE (BeNeFIT)

UNKNOWN

Sponsor Role collaborator

Leiden University Medical Center

OTHER

Sponsor Role lead

Responsible Party

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wcpeul

Professor and Chair Neurosurgery

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Leiden University Medical Center (LUMC)

Leiden, South Holland, Netherlands

Site Status

Countries

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Netherlands

References

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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.

Reference Type DERIVED
PMID: 35351178 (View on PubMed)

Other Identifiers

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NL72116.058.20/P20.005

Identifier Type: -

Identifier Source: org_study_id

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