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Clinical Trials in Canada / NCT06429332
Recruiting Phase 4

International Care Bundle Evaluation in Cerebral Hemorrhage Research

NCT06429332 · tracked via the Priya Life Science Canada tracker
Phase
Phase 4
Started
2025-01-07
Last updated
2026-05-22

Condition(s) studied

Intracerebral HemorrhageIntracerebral HaemorrhageIntraventricular HemorrhageStrokeCerebrovascular Disease

Investigational drug(s) / intervention(s)

Reversal of Oral anticoagulation within 30 minutesEarly intensive blood pressure loweringTreatment of pyrexiaHyperglycemia treatmentDo-not-resuscitate (DNR) or withdrawal of careReferral to Intensive CareReferral to NeurosurgeryRepeat brain imagingStandard care

Reversal of Oral anticoagulation within 30 minutes: In situations of either an elevated INR with the use of warfarin - treatment with either 3- or 4-factor prothrombin complex concentrate (PCC) or fresh frozen plasma (FFP) within 30 minutes of ICH diagnosis on NCCT to reach and maintain an INR target \<1.3; or where there has been recent use (\<48 hours) of a direct oral anticoagulant (DOAC), use of an appropriate reversal agent within 30 minutes, where available, and according to local approvals.

Early intensive blood pressure lowering: A systolic blood pressure (BP) target of 130-140 mmHg within 30 minutes of ICH diagnosis on NCCT is strived for, and to maintain this BP level for the first 7 days (for patients presenting with blood pressure \<200 mmHg). If blood pressure ≥200 and \<220, a target BP of 160 mmHg should be targeted at 30 minutes, and 130-140 mmHg should be achieved in 60 minutes. If BP ≥220, target BP of 160 mmHg and should be achieved in 60 minutes.

Treatment of pyrexia: To achieve a body temperature target \<37.5 °C within the first 24h following ICH diagnosis on NCCT

Hyperglycemia treatment: To maintain a blood glucose level 7-10 mmol/L within the first 24h following ICH diagnosis on NCCT

Do-not-resuscitate (DNR) or withdrawal of care: Refrain from the use of DNR or withdrawal of care orders for 48 hours

Referral to Intensive Care: Immediate (\<30 min) referral to intensive care if airway, breathing and/or circulation are compromized

Referral to Neurosurgery: Immediate (\<30 min) referral to neurosurgery if any of the following criteria are fulfilled: * Large and/or rapidly evolving supratentorial ICH (\>20 ml volume) * Any intraventricular extension * Posterior fossa bleed, irrespective of volume * Suspicion of a vascular malformation, independent of volume or location * Reduction in reaction to sensory stimulation or drowsiness

Repeat brain imaging: Repeat 6-12-hour brain imaging with the physicians choice of modality, preferably computed tomography (CT), if clinical deterioration or the patient received OAC reversal treatment

Standard care: For patients in the usual-care group, decisions about the location of care delivery, investigations, monitoring, and all treatments are made by the treating clinical team. Data will be collected regarding the management of patients, including insertion of invasive monitoring devices, intravenous fluid resuscitation, BP lowering, vasoactive support, glycemic control, mechanical ventilation, neurosurgery, and other supportive therapy.

Study summary

Spontaneous intracerebral haemorrhage (ICH) accounts for approximately 10-15% of all strokes but stands for 50% of stroke-related morbidity and mortality. Approximately half of all patients with ICH have a decreased level of consciousness at hospital admission. Despite this, intensive care and neurosurgical interventions are uncommon. A study conducted in low- and middle-income countries has demonstrated a beneficial effect of a treatment package consisting of early intensive blood pressure lowering, as well as the treatment of pyrexia and elevated blood glucose levels. The I-CATCHER team is now planning to conduct a similar study in Sweden and Australia, as well as in other high-income countries. The study has a clear focus on implementation, aiming to improve treatment and prognosis for patients with ICH within a few years. The purpose of I-CATCHER is to investigate whether a structured treatment package (Care Bundle) improves 3-month prognosis in patients with spontaneous ICH compared to standard care.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults (age ≥18 years) * Non-contrast computerized tomography (NCCT) imaging-verified diagnosis of spontaneous intracerebral haemorrhage * ≤24 hours from symptom onset or presumed symptom onset (last seen well) Exclusion Criteria: * Previous care limitation * End-stage comorbidity with short life-expectancy (\<6 m; e.g. terminal cancer) * ICH caused by brain tumor or cerebral venous thrombosis * Clinical signs of brain herniation at first presentation (unresponsive patient with bilaterally fixed, maximally dilated pupils) * Pregnant women beyond 22 weeks gestation may only be included after thorough discussion with an obstetrician to determine risks vs benefit.

Primary outcome measure(s)

Trial sites (54)

FacilityCityRegionStatus
The University of Oklahoma Health Oklahoma City Oklahoma Recruiting
Royal Adelaide Hospital Adelaide Australia Recruiting
Monash Medical Centre Clayton Australia Recruiting
The George Institute for Global Health Sydney Australia Not Yet Recruiting
Health Sciences North/Health Sciences North Research Institute Greater Sudbury Ontario Recruiting
Hamilton General Hospital Hamilton Ontario Recruiting
Ottawa Hospital Research Institute Ottawa Ontario Recruiting
Hong Kong University Hospital Hong Kong Hong Kong Recruiting
Landspitali University Hospital Reykjavik Iceland Recruiting
Avezzano Ospedale SS. Filippo e Nicola Avezzano Italy Recruiting
Citta di Castello Ospedale Città di Castello Città di Castello Italy Recruiting
Gubbio Ospedale di Gubbio e Gualdo Tadino Gubbio Italy Recruiting
Azienda Ospedaliera Santa Maria della Misericordia Perugia Perugia Italy Recruiting
Roma Policlinico Gemelli Roma Italy Recruiting
National University of Malaysia Hospital Kuala Lumpur Malaysia Recruiting
Universiti Putra Malaysia Hospital Serdang Malaysia Recruiting
Höglandssjukhuset i Eksjö Eksjö Sweden Recruiting
Sahlgrenska Universitetssjukhuset Gothenburg Sweden Recruiting
Östra Sjukhuset Gothenburg Sweden Recruiting
Hässleholms Sjukhus Hässleholm Sweden Recruiting
Helsingborgs Lasarett Helsingborg Sweden Recruiting
Karolinska Universitetssjukhuset Huddinge Huddinge Sweden Recruiting
Länssjukhuset Ryhov Jönköping Sweden Recruiting
Länssjukhuset Kalmar Kalmar Sweden Recruiting
Blekingesjukhuset Karlskrona Karlskrona Sweden Recruiting
Blekingesjukhuset Karlskrona Sweden Recruiting
Centralsjukhuset Karlstad Karlstad Sweden Recruiting
Västmanlands sjukhus Köping Köping Sweden Recruiting
Centralsjukhuset Kristianstad Kristianstad Sweden Recruiting
Kungälvs sjukhus Kungälv Sweden Recruiting
Univeristetssjukhuset Linköping Linköping Sweden Recruiting
Ljungby Lasarett Ljungby Sweden Recruiting
Skåne University Hospital Lund Neurosurgery dept Lund Sweden Recruiting
Skåne University Hospital Lund Lund Sweden Recruiting
Region Skåne, Skåne University Hospital in Malmö, Department of Neurology Malmö Sweden Recruiting
Mölndals Sjukhus Mölndal Sweden Recruiting
Oskarshamn Sjukhus Oskarshamn Sweden Recruiting
Universitetssjukhuset Örebro Örebro Sweden Recruiting
Östersunds Lasarett Östersund Sweden Recruiting
Skaraborgs Sjukhus Skövde Skövde Sweden Recruiting

+ 14 more sites — see the full list on the official registry below.

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06429332 on ClinicalTrials.gov ↗ ← All trials in Canada