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Clinical Trials in Italy / NCT06465758
Recruiting Observational

Prognostic Recovery Observations and Guidance for Evaluating Stroke Survivors

NCT06465758 · tracked via the Priya Life Science Italy tracker
Sponsor
IRCCS San Raffaele
Phase
Observational
Started
2024-05-21
Last updated
2024-06-20

Condition(s) studied

Acute StrokeFunctional RecoveryPrognostic Factors

Study summary

This research delves into the acute prognostic factors influencing functional recovery in individuals who have experienced a stroke. The objective is to describe patterns of functional recovery after a stroke and identify new, clinically significant outcomes or metrics that can serve as predictive indicators for post-stroke functional recovery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 * Haemorrhagic or ischaemic stroke confirmed by a clinical diagnosis and by brain imaging * NIHSS item 5-6 ≥1 * 3 to 10 days post-stroke Exclusion Criteria: * Transient ischaemic attack * Premorbid Modified Rankin Scale ≥ 4 * Acute orthopaedic complications * Inability to give informed consent

Primary outcome measure(s)

  • Action Research Arm Test (ARAT) — Within 3-10 days post stroke and at the three-month, six-month and one-year follow-up
    To evaluate upper limb functional recovery. The score ranges from 0 (indicating low functional recovery) to 57 (high functional recovery).

Trial sites (1)

FacilityCityRegionStatus
IRCCS San Raffaele Milan Italy Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06465758 on ClinicalTrials.gov ↗ ← All trials in Italy