Cilostazol With Nimodipine to Improve Outcome After Aneurysmal Subarachnoid Hemorrhage

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier St Anne

About this trial

The CASH study is a randomized, double-blind, placebo-controlled trial evaluating whether adding cilostazol to standard nimodipine therapy improves neurological outcomes in patients with aneurysmal subarachnoid hemorrhage (aSAH). The primary objective is to assess functional outcome at 6 months using the modified Rankin Scale. A total of 630 patients will be enrolled within 96 hours of aSAH onset and treated for 14 days. The study is conducted across 9 centers in France, funded by a PHRC, and overseen by an independent monitoring board.

Eligibility criteria

Qualifiers

Adult patients admitted to an ICU with SAH related to a ruptured cerebral aneurysm occurring within the last 96 hours.

Aneurysm successfully secured by surgical clipping or endovascular coiling

Consent of the patient or, if not possible, from a proxy (emergency clause).

Registration in a national health care system

Disqualifiers

- Precritical modified Rankin Scale (mRS) > 2

Nonaneurysmal SAH

Delayed >96h admission after first symptoms of SAH

Coma defined by GCS of 3-5 with untreatable aneurysm will be excluded"

Trial design

Treatments tested in this trial

  • Cilostazol (Pletal®) 100 mg Tablets
  • Placebo
  • Nimodipine group

Treatment groups

630 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators