NCT07500116Recruiting
NORA-HOME: An Ambulatory Multimodal Monitoring Model In Patients With Minor Stroke And Transient Ischemic Attacks
NORA-HOME. Efficiency And Safety An Ambulatory Multimodal Monitoring Model In Patients With Minor Stroke And Transient Ischemic Attacks
Source: ClinicalTrials.gov · Last updated 30 Mar 2026
Brief summary (registry, in English)
In this project, we aim to validate a Home Hospitalization plan for patients with TIA or minor stroke. Our hypothesis is that our Multimodal Home Hospitalization program (NORAHOME) for patients with TIA and minor stroke is safe, reduces the complications associated with conventional hospitalization, and is more efficient than Standard Clinical Practice. To conduct the study, we require the voluntary participation of patients with TIA and minor strokes.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 250 (estimated)
- First submitted
- 11 Mar 2026
- Start date
- Jan 2025
- Primary completion date
- Jun 2027
- Lead sponsor
- Hospital Universitari Vall d'Hebron Research Institute
- Diseases
- Stroke
- NCT number
- NCT07500116
What you commit to
- Study type: Interventional
- Planned participants: 250
- From Jan 2025 to the primary completion date, Jun 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.
Other illness
- Patients with pre-existing neurological or psychiatric conditions that may interfere with or complicate follow-up and evaluations.
- Clinical (terminal condition) or social (language barrier) impossibility to complete follow-up assessments.
Other
- Severe stenosis or symptomatic arterial occlusion requiring admission for potential reperfusion and/or arterial revascularization treatments.
Who the study is looking for
- Age \>18 years.
- Availability of a smartphone for the patient or caregiver.
- Family support and/or formal caregiver.
- Clinical stability during the last 12 hours in the Emergency Department.
- Signed informed consent by the patient and/or family member or legal representative.
Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Vall Hebron University Hospital Coordinator of this site? Confirm its status | Barcelona | Spain | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.