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NCT06429332RecruitingPhase 4

International Care Bundle Evaluation in Cerebral Hemorrhage Research

International Care Bundle Evaluation in Cerebral Hemorrhage Research - a Batched Parallel Cluster-randomized Trial With a Baseline Period

Source: ClinicalTrials.gov · Last updated 22 May 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
3500 (estimated)
First submitted
14 May 2024
Start date
7 Jan 2025
Primary completion date
1 Mar 2027
Lead sponsor
Region Skane
Diseases
Stroke
NCT number
NCT06429332

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 3500
  • From 7 Jan 2025 to the primary completion date, 1 Mar 2027
  • 54 sites in 8 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous care limitation

Other illness

  • End-stage comorbidity with short life-expectancy (\<6 m; e.g. terminal cancer)
  • ICH caused by brain tumor or cerebral venous thrombosis

Other

  • 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.

Who the study is looking for

  • 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)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (54)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Royal Adelaide Hospital
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AdelaideAustraliaRecruiting
Monash Medical Centre
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ClaytonAustraliaRecruiting
The George Institute for Global Health
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SydneyAustraliaNot yet recruiting
Health Sciences North/Health Sciences North Research Institute
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Greater SudburyCanadaRecruiting
Hamilton General Hospital
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HamiltonCanadaRecruiting
Ottawa Hospital Research Institute
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OttawaCanadaRecruiting
Hong Kong University Hospital
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Hong KongHong Kong SAR ChinaRecruiting
Landspitali University Hospital
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ReykjavikIcelandRecruiting
Avezzano Ospedale SS. Filippo e Nicola
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AvezzanoItalyRecruiting
Citta di Castello Ospedale Città di Castello
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Città di CastelloItalyRecruiting
Gubbio Ospedale di Gubbio e Gualdo Tadino
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GubbioItalyRecruiting
Azienda Ospedaliera Santa Maria della Misericordia Perugia
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PerugiaItalyRecruiting
Roma Policlinico Gemelli
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RomaItalyRecruiting
National University of Malaysia Hospital
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Kuala LumpurMalaysiaRecruiting
Universiti Putra Malaysia Hospital
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SerdangMalaysiaRecruiting
Höglandssjukhuset i Eksjö
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EksjöSwedenRecruiting
Sahlgrenska Universitetssjukhuset
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GothenburgSwedenRecruiting
Östra Sjukhuset
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GothenburgSwedenRecruiting
Hässleholms sjukhus
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HässleholmSwedenRecruiting
Helsingborgs lasarett
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HelsingborgSwedenRecruiting
Karolinska Universitetssjukhuset Huddinge
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HuddingeSwedenRecruiting
Lanssjukhuset Ryhov
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JönköpingSwedenRecruiting
Länssjukhuset Kalmar
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KalmarSwedenRecruiting
Blekingesjukhuset Karlskrona
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KarlskronaSwedenRecruiting
Blekingesjukhuset
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KarlskronaSwedenRecruiting
Centralsjukhuset Karlstad
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KarlstadSwedenRecruiting
Västmanlands sjukhus Köping
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KöpingSwedenRecruiting
Centralsjukhuset Kristianstad
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KristianstadSwedenRecruiting
Kungälvs sjukhus
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KungälvSwedenRecruiting
Univeristetssjukhuset Linköping
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LinköpingSwedenRecruiting
Ljungby Lasarett
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LjungbySwedenRecruiting
Skåne University Hospital Lund
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LundSwedenRecruiting
Skåne University Hospital Lund Neurosurgery dept
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LundSwedenRecruiting
Region Skåne, Skåne University Hospital in Malmö, Department of Neurology
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MalmöSwedenRecruiting
Mölndals Sjukhus
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MölndalSwedenRecruiting
Universitetssjukhuset Örebro
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ÖrebroSwedenRecruiting
Oskarshamn Sjukhus
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OskarshamnSwedenRecruiting
Östersunds Lasarett
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ÖstersundSwedenRecruiting
Skaraborgs sjukhus Skövde
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SkövdeSwedenRecruiting
Södersjukhuset
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StockholmSwedenRecruiting
Capio St Görans sjukhus
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StockholmSwedenRecruiting
Karolinska Universitetssjukhuset Solna
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StockholmSwedenRecruiting
Danderyds sjukhus
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StockholmSwedenRecruiting
Länssjukhuset Sundsvall
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SundsvallSwedenRecruiting
Norra Älvsborgs Länssjukhus
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TrollhättanSwedenRecruiting
Norrlands universitetssjukhus
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UmeåSwedenRecruiting
Akademiska Sjukhuset Uppsal
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UppsalaSwedenRecruiting
Lasarettet i Enköping
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UppsalaSwedenRecruiting
Hallands sjukhus Varberg
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VarbergSwedenRecruiting
Värnamo sjukhus
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VärnamoSwedenRecruiting
Västerås
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VästeråsSwedenRecruiting
Centrallasarettet Växjö
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VaxjoSwedenRecruiting
Ystads lasarett
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YstadSwedenRecruiting
The University of Oklahoma Health
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Oklahoma CityUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.