Observational Study of Patients With Subarachnoid Hemorrhage

A Prospective, Observational Registry of Patient With Subarachnoid Hemorrhage in Neurocritical Care Unit

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02890004

Acronym

ProReSHA

Enrollment

1000

Registered

2016-09-07

Start date

2017-02-16

Completion date

2020-03-16

Last updated

2018-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Subarachnoid Hemorrhage

Keywords

Subarachnoid Hemorrhage, Neurointensive care, Observational registry

Brief summary

This prospective, observational study aim to identify : * Prognostic factor of patients with subarachnoid haemorrhage in neuro intensive care unit * The impact of standard therapeutic used (surgery, embolization ; medical treatment of vasospasm ; treatment of complications like hyponatremia, stress myocardiopathy, …)

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Subarachnoid hemorrhage

Exclusion criteria

* None

Design outcomes

Primary

Measure	Time frame
Survival	at day 0

Secondary

Measure	Time frame	Description
Neurological outcome with the Glasgow Coma Scale (GCS) score	at day 0	—
Neuropsychological outcome with the Montreal Cognitive Assessment (MoCA) score	at day 0	—
Brain lesions with MRI	at day 0	—
delay of apparition of hyponatremia	on alternte days after Day 0	Natremia in standard blood sample, Natremia is routinelly evaluated on alternte days, and more if required.

Countries

France

Contacts

Primary ContactFrédéric DAILLER, MD

frederic.dailler@chu-lyon.fr4 72 35 75 76

Outcome results