Fact CheckerSign in

NCT06805929Recruiting

Correlation Between Clinical Neurological Biomarkers and Rehabilitation Outcome

Correlation Study Between Clinical, Neurophysiological, and Neuroradiological Biomarkers and Rehabilitation Outcomes to Predict Functional Recovery After Stroke and Personalize Treatment.

Source: ClinicalTrials.gov · Last updated 4 Nov 2026

Brief summary (registry, in English)

Our study purpose is to evaluate the predictive power of various clinical, neurophysiological, and neuroimaging biomarkers-acquired and analyzed using advanced and integrated techniques-on motor functional recovery and disability post-stroke. The goal is to construct an integrated individual biomarker algorithm with a high predictive value for outcomes.

Status (registry)
Recruiting
Study type
Observational
Enrollment
300 (estimated)
First submitted
28 Jan 2025
Start date
15 Jun 2020
Primary completion date
31 Dec 2027
Lead sponsor
IRCCS San Raffaele Roma
Diseases
Stroke
NCT number
NCT06805929

What you commit to

  • Study type: Observational
  • Planned participants: 300
  • From 15 Jun 2020 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous stroke.

Other illness

  • Stroke in territories other than the middle cerebral artery.
  • History of cancer in the past two years.
  • Presence of other neurological conditions interfering with biomarkers

Other

  • Inability to provide informed consent.
  • Contraindications to TMS or MRI.

Who the study is looking for

  • First stroke in the middle cerebral artery territory.
  • Ischemic or hemorrhagic stroke (7-30 days post-acute event).
  • Upper limb plegia or paresis.
  • Both genders, aged \>18 years.
  • Ability to provide informed consent by the patient or caregiver/responsible relative.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
IRCCS San Raffaele
Coordinator of this site? Confirm its status
RomaItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.