SWITCH: Decompressive Hemicraniectomy in Intracerebral Hemorrhage

Sponsor
University Hospital Inselspital, Berne (Other)
Overall Status
Recruiting
CT.gov ID
NCT02258919
Collaborator
(none)
300
37
2
107
8.1
0.1

Study Details

Study Description

Brief Summary

Spontaneous intracerebral hemorrhage (ICH) remains a devastating disease with mortality rates up to 52% at 30 days. It is a major public health problem with an annual incidence of 10-30 per 100'000 population, accounting for 2 million (10-15%) of about 15 million strokes worldwide each year. The strategy of decompressive craniectomy (DC) is beneficial in patients with malignant middle cerebral artery (MCA) infarction. Based on the common pathophysiological mechanisms of these two conditions, this procedure is also frequently performed in patients with ICH, but is has not yet been investigated in a randomized trial.

The primary objective of this randomized controlled trial is to determine whether decompressive surgery and best medical treatment in patients with spontaneous ICH will improve outcome compared to best medical treatment only.

Secondary objectives are to analyze mortality, dependency and quality of life. Safety endpoints are to determine cause of any mortality and the rate of medical and surgical complications after DC compared with best medical treatment alone.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Decompressive craniectomy (DC) and best medical treatment
  • Procedure: Best medical treatment
N/A

Detailed Description

Background

Spontaneous intracerebral hemorrhage (ICH) remains a devastating disease with mortality rates up to 52% at 30 days. It is a major public health problem with an annual incidence of 10-30 per 100'000 population, accounting for 2 million (10-15%) of about 15 million strokes worldwide each year. One-third of patients with ICH die within one month and the majority of survivors remain handicapped. Neurological injury resulting from ICH is mediated by the mass effect of the hematoma, secondary to brain edema and/or both mechanisms. Treatment of ICH is one of the major unresolved issues of acute stroke treatment. The International Surgical Trials in Intracerebral Hemorrhage (STICH and STICH II) and other randomized controlled trials did not show any superiority of surgical treatment compared to conservative treatment approaches. Nevertheless, surgical treatment in ICH remains a matter of debate and attempts to improve outcome using surgical therapy are still ongoing. Many efforts are made to minimize the invasiveness of operative procedures such as clot evacuation. However, direct surgical interventions aiming at the removal of the hematoma have failed to improve neurological outcome for most subtypes of ICH, especially deep-seated hematomas. The trauma of open craniotomy and especially trauma to the brain parenchyma for hematoma evacuation are considered to outweigh the benefits of surgery.

Decompressive craniectomy (DC), which is beneficial in patients with malignant middle cerebral artery (MCA) infarction, may indirectly relieve the mass effect, decrease perihematomal tissue pressure, improve blood flow, reduce secondary brain damage and improve outcome without further damage to the brain due to surgery. Consequently, DC has been established as a standard surgical therapy for patients with malignant MCA infarction with a level of evidence grade 2. Decompressive craniectomy for acute stroke is one of the most effective treatments available: the number needed to be treated to save one patient's life is 2. Decompressive craniectomy is also a standard therapeutic procedure in patients with ICH due to sinus venous thrombosis, herpes encephalitis, or ruptured intracranial aneurysms. In patients with traumatic brain injury DC is a standard therapy to reduce elevated intracranial pressure. The investigators and others assessed whether DC is feasible and beneficial in patients with spontaneous intracranial hemorrhage. The investigators showed in a previous retrospective trial that DC in patients with supratentorial ICH is safe and feasible and may reduce mortality compared to matched controls with best medical treatment alone. The limitations of the feasibility trial are its retrospective design, the small sample size and the inhomogeneity of the patient cohort with respect to the origin of ICH. Furthermore, in the feasibility trial the decision for DC was taken on an individual basis rather than according to a strict protocol, introducing a potential selection bias. Nevertheless, the preliminary results are encouraging. Recently, three human trials, one animal study, one meta-analysis, and one original contribution have been published on this topic. However, no prospective randomized trial has ever assessed whether DC without hematoma evacuation in patients with acute ICH improves outcome. All recent studies showed promising results and all call for the initiation of a randomized controlled trial.

Objective

The primary objective of this randomized controlled trial is to determine whether decompressive surgery and best medical treatment in patients with spontaneous ICH will improve outcome compared to best medical treatment only.

Secondary objectives are to analyze mortality, dependency and quality of life. Safety endpoints are to determine cause of any mortality and the rate of medical and surgical complications after DC compared with best medical treatment alone.

Methods

All patients with a suspected intracerebral hemorrhage will be considered for this trial. Randomization of eligible patients will be performed within 66 hours after ictus in patients with stable clot volume and surgery no later than 6 hours after randomization. Patients randomized to the control group will receive best medical treatment according to international guidelines. Patients randomized to the treatment group will receive best medical treatment and a DC of at least 12cm according to institutional guidelines and a surgical protocol. The primary outcome death and dependency at 6 months will be assessed by a trained person unaware of treatment allocation. Favorable outcome is defined as a modified Rankin Scale (mRS) score of 0 to 4, poor outcome as modified Rankin Scale score of 5 or 6.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Swiss Trial of Decompressive Craniectomy Versus Best Medical Treatment of Spontaneous Supratentorial Intracerebral Hemorrhage (SWITCH): a Randomized Controlled Trial
Study Start Date :
Oct 1, 2014
Anticipated Primary Completion Date :
Mar 1, 2023
Anticipated Study Completion Date :
Sep 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Decompressive craniectomy and best medical treatment

Decompressive craniectomy and best medical treatment

Procedure: Decompressive craniectomy (DC) and best medical treatment
Decompressive craniectomy: All patients in the treatment group will receive DC of at least 12 cm according to institutional guidelines and a published surgical protocol. Best medical treatment: Best medical treatment is based on American Heart Association/American Stroke Association (AHA/ASA) and European Stroke Organisation (ESO) as published in the current protocol from 2010 and 2014 respectively.

Active Comparator: Best medical treatment

Best medical treatment

Procedure: Best medical treatment
Best medical treatment is based on American Heart Association/American Stroke Association (AHA/ASA) and European Stroke Organisation (ESO) as published in the current protocol from 2010 and 2014 respectively.

Outcome Measures

Primary Outcome Measures

  1. Score in modified Rankin Scale (mRS) [6 months]

    Assessed by telephone interview

Secondary Outcome Measures

  1. Mortality [7 days, 30 days, 180 days, 12 months]

  2. mRS score of 0-3 versus 4-6 [30 days, 180 days, 12 months]

  3. Categorical shift in mRS score [180 days, 12 months]

  4. Quality of life [180 days, 12 months]

  5. Death and intracranial hemorrhage [intraoperative]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Written informed consent of the patient or of patient's next of kin plus consent of an independent physician if patient is unable to consent before randomization

  • Acute stroke syndrome due to a spontaneous ICH, defined as the sudden occurrence of bleeding into the parenchyma of the basal ganglia and/or thalamus that may extend into the ventricles and into the cerebral lobes, and into the subarachnoid space, confirmed by clinical history and imaging

  • Age: ≥18 to ≤75 years

  • Glasgow coma scale (GCS) <14 and >7

  • Neurological deficit with a NIHSS score of ≥10 and ≤30

  • Able to be randomly assigned to surgical treatment within 66 hours after ictus

  • Surgery performed not later than 6 hours after randomization

  • Volume of hematoma ≥30 ml and ≤100 ml

  • Stable clot volume

  • International normalized ratio (INR) <1.5, thrombocytes >100 T/ml

Exclusion Criteria

  • ICH due to known or suspected structural abnormality in the brain (e.g., intracranial aneurysm, brain arteriovenous malformation, brain tumor) or brain trauma, or previous stroke thrombolysis

  • Cerebellar or brainstem hemorrhage

  • Exclusive lobar hemorrhage

  • Known advanced dementia or significant pre-stroke disability

  • Concomitant medical illness that would interfere with outcome assessment and follow-up

  • Randomization not possible within 66 hours after ictus

  • Pregnancy

  • Prior major brain surgery within <6 month or prior DC

  • Foreseeable difficulties in follow-up due to geographic reasons

  • Known definite contraindication for a surgical procedure

  • A very high likelihood that the patient will die within the next 24 hours on the basis of clinical and/or radiological criteria

  • Previous participation in this trial or in another ongoing investigational trial

  • Prior symptomatic ICH

  • ICH secondary to thrombolysis

  • Bilateral areactive pupils

Contacts and Locations

Locations

Site City State Country Postal Code
1 Universitätsklinik für Neurochirurgie, Medizinische Universität Innsbruck Innsbruck Austria 6020
2 Universitätsklinik für Neurochirurgie, Kepler Universitätsklinikum Linz Linz Austria 4020
3 Cliniques Universitaires Saint Luc Bruxelles Belgium 1200
4 UZ Leuven Leuven Belgium 3000
5 Department of Neurology, Helsinki University Central Hospital Helsinki Finland 00290
6 Centre Hospitalier Universitaire de Caen Caen France 14033
7 Fondation Adolphe de Rothschild Paris France 75019
8 Klinik für Neurochirurgie, Universitätsklinikum Schleswig Holstein Lübeck Schleswig Holstein Germany 23562
9 Klinik für Neurochirugie, Helios Klinikum Erfurt Erfurt Thüringen Germany 99089
10 Klinik für Neurochirurgie Uniklinik RWTH Aachen Aachen Germany 52074
11 Department of Neurosurgery, Charité - Universitätsmedizin Berlin Berlin Germany 13353
12 Klinik und Poliklinik für Neurochirurgie, Universitätsklinikum Bonn Bonn Germany 53127
13 Klinik für Neurochirurgie, Universitätsklinikum Düsseldorf Düsseldorf Germany 40225
14 Neurologische Klinik, Universitätsklinikum Erlangen Erlangen Germany 91054
15 Klinik für Neurochirurgie, Universitätsklinikum Essen (AöR) Essen Germany 45147
16 Zentrum der Neurologie und Neurochirurgie, Universitätsklinikum Frankfurt Frankfurt Germany 60590
17 Klinik für Neurochirurgie, Universitätsklinikum Freiburg Freiburg Germany 79106
18 Neurochirurgische Klinik, Universitätsklinikum Gießen und Marburg UKGM Gießen Germany 35392
19 Klinik für Neurochirurgie, Universitätsmedizin Göttingen Göttingen Germany 37075
20 Klinik für Neurochirurgie, Klinikum Kassel Kassel Germany 34125
21 Neurochirurgische Klinik, Universitätsmedizin Mainz Mainz Germany 55116
22 Neurochirurgische Klinik, Universitätsklinikum Mannheim Mannheim Germany 68167
23 Dep. of Neurosurgery, Klinikum rechts der Isar der Technischen Universität München Munich Germany 81675
24 Klinik für Allgemeine Neurologie, Universitätsklinikum Münster Münster Germany 48149
25 Klinik für Neurochirurgie, Universitätsklinikum Würzburg Würzburg Germany 97080
26 Academic Medical Center Amsterdam, Department of Neurology Amsterdam Netherlands 1105
27 University Medical Center Utrecht, Department of Neurology, Department of Neurosurgery Utrecht Netherlands 3584
28 Servicio de Neurocirurgía Hospital de la Santa Creu i Sant Pau Barcelona Spain 08041
29 Servicio de Neurocirurgía Bellvitge Hospital Barcelona Spain 08907
30 Servicio de Neurología, Hospital Universitario La Paz Madrid Spain 28046
31 Servicios de Neurología, Neurocirugía y Cuidados Intensivos del Hospital Virgen del Rocío Sevilla Spain 41013
32 Sahlgrenska University Hospital Gothenburg Sweden 41345
33 Dep. of Neurology / Dep. of Neurosurgery, Bern University Hospital Bern Switzerland 3010
34 Dep. of Clinical Neuroscience, Service of Neurosurgery Geneva Switzerland 1211
35 Dep. of Neurosurgery, Kantonsspital Luzern Lucerne Switzerland 6000
36 Dep. Neurosurgery, Ospedale Regionale di Lugano Lugano Switzerland 6903
37 Dep. of Neurosurgery, University Hospital Zürich Zürich Switzerland 8091

Sponsors and Collaborators

  • University Hospital Inselspital, Berne

Investigators

  • Study Director: Urs Fischer, Prof. Dr. med., Dep. of Neurology, Inselspital Bern
  • Study Chair: Jürgen Beck, Prof. Dr. med., Dep. of Neurosurgery, Inselspital Bern

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
University Hospital Inselspital, Berne
ClinicalTrials.gov Identifier:
NCT02258919
Other Study ID Numbers:
  • 163/14
  • 32003B_150009
First Posted:
Oct 8, 2014
Last Update Posted:
Jun 5, 2020
Last Verified:
Jun 1, 2020
Keywords provided by University Hospital Inselspital, Berne
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 5, 2020