Optimizing care for patients with non-traumatic intracerebral hemorrhage

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to evaluate the management of patients with non-traumatic intracerebral hemorrhage (ICH) at the University Hospital of Tours. It includes a retrospective analysis of patients admitted between 2018-2021 and a prospective evaluation of current management practices. The study focuses on implementing a standardized protocol for emergency care, including rapid imaging, antihypertensive treatment, and follow-up evaluations. The goal is to improve patient outcomes by analyzing and optimizing the acute management of ICH.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* aged over 18 years
* emergency admission to the University Hospital of Tours
* having an ICH on imaging performed upon admission (CT scan or MRI) at the University Hospital of Tours

Exclusion criteria :

\- Patient who has given their opposition to the collection of their data

Where it's running

• University Hospital of Angers
  Angers, France Recruiting
• University Hospital of Poitiers
  Poitiers, France Recruiting
• University Hospital Center of Tours
  Tours, France Recruiting

Study contacts

• Principal investigator: Marco PASI, MD, PHD — neurovascular unit, neurology department, CHRU Tours
• Study coordinator: Marco PASI, MD, PHD
• Email: M.PASI@chu-tours.fr
• Phone: +33 0247478024

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• AI-based tools to help diagnose, treat and predict stroke outcomes across multiple hospitals

  This study tests AI-powered tools on real-world stroke patients to see if they can improve pre-hospital triage, diagnosis, and outcome prediction while data stay securely within each hospital.

  Recruiting at 2 sites Hospital Universitari Vall d'Hebron Research Institute · Leuven and 6 other locations · NCT07924371

• Smartphone-based EEG to detect hidden awareness in ICU patients with brain injuries

  Researchers will test a smartphone-enabled EEG to see if it can reveal Cognitive Motor Dissociation in ICU patients who can’t show commands at bedside.

  Recruiting Columbia University · Miami, Florida and 8 other locations · NCT07917728

• Chinese multicenter group studies spontaneous intracerebral hemorrhage in adults

  This study tests how a large group of adults with spontaneous intracerebral hemorrhage (and a healthy control group) progress over time to understand outcomes and determinants of recovery.

  Recruiting Xiangya Hospital of Central South University · Changsha, Hunan · NCT07833410

• Rapid Evacuation and Access of Cerebral Hemorrhage Registry: observing minimally invasive surgery outcomes

  This registry collection tests how minimally invasive brain-bleed procedures work in real patients with acute spontaneous intracerebral hemorrhage.

  Recruiting Emory University · Atlanta, Georgia · NCT07651631

• Single triple-combination blood pressure pill after intracerebral hemorrhage

  This trial tests whether a single pill combining amlodipine, valsartan, and hydrochlorothiazide helps adults who recently had an intracerebral hemorrhage control their blood pressure.

  Recruiting The University of Hong Kong · Hong Kong, Hong Kong and 3 other locations · NCT07458880

• Vitamin D treatment after intracerebral hemorrhage

  This will try giving higher-dose vitamin D to adults within 96 hours of an intracerebral hemorrhage to see if it helps clear the bleed faster and is safe.

  Recruiting The University of Hong Kong · Hong Kong · NCT07458815

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.