← Eichor
Study identifier: NCT06804421 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Diagnosis and Treatment of Late Neurological Ischemic Deficit in Patients Suffering From Subarachnoid Hemorrhage.

Condition: Aneurysmal Subarachnoid Haemorrhage · Delayed Ischemic Neurological Deficit  ·  Sponsor: Fondazione IRCCS San Gerardo dei Tintori

PhaseN/A
Planned participants1400
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Recent studies state that patients affected by aneurysmal subarachnoid hemorrhage (aSAH) today survive longer because they are treated early. Unfortunately, patients often develop chronic disabling neurological deficits at a rate that is still unacceptable given the progress in the specific treatment of this pathology and the volume of systems of neurological monitoring available to date in Italy. The main cause of unfavorable neurological outcome is delayed cerebral ischemia (DCI), often resulting from symptomatic vasospasm defined as delayed neurological ischemic deficit (DIND). The incidence of DIND is not defined and is difficult to diagnose early as there is no gold standard for identifying it, nor guidelines regarding the most effective treatment. Given these gaps, the primary objective of this study is to describe the incidence of DIND in patients affected by aSAH, collecting information regarding the diagnostic imaging (neurological symptom on clinical examination or alteration on instrumental monitoring). Secondary objectives will be to evaluate the different therapeutic strategies adopted in the different participating centers and compare these strategies to mortality and short- and long-term functional neurological outcome. Furthermore, as there are no data in the literature, the Investigators want to describe the indications, usefulness and intensity of treatment in the aSAH patient in case of monitoring of parenchymal intracranial pressure.

This description comes directly from the study's public registry record.

Talk to the study team

Giuseppe Citerio, Professor, Head of Department  ·  +390392334316  ·  giuseppe.citerio@unimib.it

Clinical Research Coordination Office  ·  +390392339583  ·  ricerca.clinica@irccs-sangerardo.it

Always discuss trial participation with your own doctor first.

Locations (33)

ASST Papa Giovanni XXIIIBergamo, BG, ItalyNot Yet Recruiting
IRCCS Istituto delle Scienze NeurologicheBologna, BO, ItalyNot Yet Recruiting
ASST Spedali CiviliBrescia, BS, ItalyNot Yet Recruiting
Fondazione PoliambulanzaBrescia, BS, ItalyNot Yet Recruiting
ASST Lariana Ospedale Sant'AnnaSan Fermo della Battaglia, CO, ItalyNot Yet Recruiting
ASST CremonaCremona, CR, ItalyNot Yet Recruiting
Azienda Ospedaliero-Universitaria CareggiFlorence, FI, ItalyNot Yet Recruiting
IRCCS Ospedale Policlinico San MartinoGenova, GE, ItalyNot Yet Recruiting
ASST Lecco - Ospedale A. ManzoniLecco, LC, ItalyNot Yet Recruiting
Fondazione IRCCS San Gerardo dei TintoriMonza, MB, ItalyRecruiting
ASST Ovest Milanese - Ospedale di LegnanoLegnano, MI, ItalyNot Yet Recruiting
ASST Fatebenefratelli SaccoMilan, MI, ItalyNot Yet Recruiting

+ 21 more locations — full list on the registry record.

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06804421