CClinicalTrials.gg
Status unknownNCT03995940HIP-REAUpdated Jun 24, 2019

Neurological Outcomes of Primary Intracerebral Haemorrhage

An observational study in Intracranial Hemorrhage, Hypertensive, sponsored by University Hospital, Grenoble. Status unknown at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-06-24.

Sponsored by University Hospital, Grenoble · Observational

The sponsor has not verified this record recently (last verified Jun 2019), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
40
Ages
18 Years and older
Sex
All
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Study summary

The main objective of this study is to determine the one-year neurological outcome of patients admitted to an intensive care unit (ICU) for a primary and spontaneous supratentorial intracerebral hemorrhages (ICH).

Read the detailed description

ICH represent a diagnostic and therapeutic emergency. ICH account for 20% of strokes with a one-year mortality of more than 45% and an uncertain neurological outcome.

For ICH patients, the main initial challenge is to determine the long term neurological outcomes and adapt the therapeutic strategy.

The majority of primary and spontaneous ICH studies involve patients in stroke units.

The study is an observational type 3 research with all the patients admitted in all the University Hospital of Grenoble Alpes ICUs between July 2012 and July 2017 for a primary and spontaneous supratentorial ICH

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Conditions studied

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In context

Cerebral Hemorrhage

476 studies on the registry are indexed under Cerebral Hemorrhage; 181 are open to participants now.

This study's planned enrollment of 40 is below the median of 275 across 180 observational studies indexed under Cerebral Hemorrhage.

Browse Cerebral Hemorrhage studies →

Lead sponsor

University Hospital, Grenoble is the lead sponsor of 815 studies on the registry; 205 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult patients with a primary and spontaneous supratentorial ICH

Inclusion criteria

  • Admission in one of the four University Hospital of Grenoble Alpes ICUs between July 2012 and July 2017 for primary and spontaneous supratentorial ICH.
  • Not opposed to participate in a research protocol (asked by phone call)

Exclusion criteria

Exclusion Criteria:

  • Pediatric patient
  • Infra-tentorials ICH
  • No spontaneous ICH (after head trauma)
  • Secondary ICH (anevrisum, arteriovenous malformation, tumor, hemorrhagic transformation, vascularitis)
  • Persons referred to in Articles L1121-5 to L1121-8 of the french public health code
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Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
40 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Neurological outcomes

    Collection of the Modified Ranking Scale (mRS) at one year by patients phone call or with the medicale file.

    Time frame: One year after the stroke

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Study locations

1 of 1 sites recruiting
  • Grenoble University Hospital
    Grenoble, 38000, France
    • Pierluigi Banco, MD · Contact · pbanco@chu-grenoble.fr · +33.4.76.76.67.29
    • Pierluigi Banco, MD · Principal investigator
    • Samuel Bersinger, MD · Sub investigator
    Recruiting
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 24, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03995940
Lead sponsor
University Hospital, Grenoble
Responsible party
Sponsor
First posted
Jun 24, 2019
Start date
Apr 30, 2019
Primary completion
Nov 2019 (estimated)
Completion
Jan 2020 (estimated)
Last update
Jun 24, 2019

Study contacts

Catherine Portal
Contact
bportal@chu-grenoble.fr
+33.4.76.76.67.29
Camille Ducki
Contact
ArcPromoteur@chu-grenoble.fr

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2019. You cannot join it, but the record below documents what was studied.

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