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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02890004
Other study ID # 69HCL16_0561
Secondary ID
Status Recruiting
Phase N/A
First received August 24, 2016
Last updated February 22, 2018
Start date February 16, 2017
Est. completion date March 16, 2020

Study information

Verified date February 2018
Source Hospices Civils de Lyon
Contact Frédéric DAILLER, MD
Phone 4 72 35 75 76
Email frederic.dailler@chu-lyon.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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, …)


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date March 16, 2020
Est. primary completion date March 16, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Subarachnoid hemorrhage

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service de réanimation polyvalente neurologique Hôpital Neurologique HCL Bron

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survival at day 0
Primary Survival at 6 months
Primary Survival at 12 months
Secondary Neurological outcome with the Glasgow Coma Scale (GCS) score at day 0
Secondary Neurological outcome with the Glasgow Coma Scale (GCS) score at 6 months
Secondary Neurological outcome with the Glasgow Coma Scale (GCS) score at 12 months
Secondary Neuropsychological outcome with the Montreal Cognitive Assessment (MoCA) score at day 0
Secondary Neuropsychological outcome with the Montreal Cognitive Assessment (MoCA) score at 6 months
Secondary Neuropsychological outcome with the Montreal Cognitive Assessment (MoCA) score at 12 months
Secondary Brain lesions with MRI at day 0
Secondary Brain lesions with MRI at 6 months
Secondary Brain lesions with MRI at 12 months
Secondary delay of apparition of hyponatremia Natremia in standard blood sample, Natremia is routinelly evaluated on alternte days, and more if required. on alternte days after Day 0
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