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Efficacy of prophylactic levetiracetam for improving functional outcome in the acute phase of intracerebral haemorrhage: a randomised, double-blind, placebo-controlled, phase 3 trial PEACH 2

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-515663-59-00
Enrollment
580
Registered
2026-04-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-02

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

Conditions

intracerebral haemorrhage

Brief summary

Functional status (death or dependency) at 6 months will be measured by the modified Rankin Scale (mRS), using ordinal logistic regression, adjusted for the stratification criterion. The mRS score will be measured during a face-to-face or remotely (if needed because of patients’ clinical status) with a standardised guided interview by a certified stroke neurologist or a certified clinical research associate (only remotely) at the 6 month-follow up visit, blinded to the patient study group.

Detailed description

number of clinical seizures within 72 h and at 1, 6 and 12 months, change in National Institute of Health Stroke Scale (NIHSS, 11 items version) score between inclusion and 72 h and 6 months., cognitive impairment assessed by the Montreal Cognitive Assessment (MoCA) version 8.3 at 6 months., Cognitive complaint assessed by the Functional Assessment of Cancer Therapy-Cognitive Function (FACT-Cog) version 3 at 6 months., Quality of life assessed by the EuroQol - 5D-5L (EQ-5D-5L) at 6 and 12 months., modified Rankin Scale (mRS) score at 12 months, Change in intracerebral haemorrhage volume (cc) and mass effect (mm) defined as midline shift on control brain imaging at 72 hours, Frequency of side effects related to treatment at 1 and 6 months, Frequency of pneumonia at 1 month, Frequency of delirium at 1 month, - anxiety and depression evaluated with the Hospital Anxiety and Depression Scale (HADS) at one and 6 months., all-cause mortality at 1, 6 and 12 months

Interventions

DRUGLévétiracetam 125mg PLACEBO
DRUGlEVETIRACETAM 100MG/ML

Sponsors

Hospices Civils De Lyon
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Functional status (death or dependency) at 6 months will be measured by the modified Rankin Scale (mRS), using ordinal logistic regression, adjusted for the stratification criterion. The mRS score will be measured during a face-to-face or remotely (if needed because of patients’ clinical status) with a standardised guided interview by a certified stroke neurologist or a certified clinical research associate (only remotely) at the 6 month-follow up visit, blinded to the patient study group.

Secondary

MeasureTime frame
number of clinical seizures within 72 h and at 1, 6 and 12 months, change in National Institute of Health Stroke Scale (NIHSS, 11 items version) score between inclusion and 72 h and 6 months., cognitive impairment assessed by the Montreal Cognitive Assessment (MoCA) version 8.3 at 6 months., Cognitive complaint assessed by the Functional Assessment of Cancer Therapy-Cognitive Function (FACT-Cog) version 3 at 6 months., Quality of life assessed by the EuroQol - 5D-5L (EQ-5D-5L) at 6 and 12 months., modified Rankin Scale (mRS) score at 12 months, Change in intracerebral haemorrhage volume (cc) and mass effect (mm) defined as midline shift on control brain imaging at 72 hours, Frequency of side effects related to treatment at 1 and 6 months, Frequency of pneumonia at 1 month, Frequency of delirium at 1 month, - anxiety and depression evaluated with the Hospital Anxiety and Depression Scale (HADS) at one and 6 months., all-cause mortality at 1, 6 and 12 months

Outcome results

None listed

Source: EU CTIS · Data processed: Apr 3, 2026