Observing recovery patterns in stroke survivors
Official title: Prognostic Recovery Observations and Guidance for Evaluating Stroke Survivors
Run by IRCCS San Raffaele · NCT06465758 · Data updated 2026-11-12
This study looks at how different factors right after a stroke affect how well survivors recover over time.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 360 (estimated) |
| Sponsor | IRCCS San Raffaele Academic / other |
| Locations | 1 site (Milan) |
| Status | Recruiting |
| Started | May 21, 2024 |
| Main results expected | May 2028 |
| Study ends | May 2029 |
| Registry record updated | June 20, 2024 |
| Trial ID | NCT06465758 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 and older who have experienced a confirmed haemorrhagic or ischaemic stroke within 3 to 10 days.
✕Probably not a fit
Patients with transient ischaemic attacks or significant pre-existing disabilities may not benefit from this study.
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 focuses on understanding the acute prognostic factors that influence functional recovery in stroke survivors. It aims to describe various recovery patterns based on clinical characteristics identified shortly after a stroke. Participants will undergo validated functional and clinical assessments at multiple time points: three months, six months, and one year post-stroke, without any interventions that could disrupt standard clinical practice. The study is conducted at the stroke unit of San Raffaele Hospital in Milan.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into predicting recovery outcomes for stroke survivors, potentially guiding personalized rehabilitation strategies.
How similar studies have gone: Other studies have shown success in identifying prognostic factors for stroke recovery, making this approach both relevant and potentially impactful.
Who can join: the full rules
Show full inclusion / exclusion criteria
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
Where it's running
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IRCCS San Raffaele
Milan, Italy Recruiting
Study contacts
- Study coordinator: Raffaella Chieffo, MD, PhD
- Email: chieffo.raffaella@hsr.it
- Phone: 0226432755
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.