NCT03962127Active, not recruiting
MIDNOR-STROKE- a Long Term Follow-up Study of Patients With First Ever Ischemic Stroke in Central Norway
MIDNOR-STROKE A Prospective Observation Study of a Cohort of 800 Patients With First Ever Ischemic Stroke in Central Norway
Source: ClinicalTrials.gov · Last updated 13 Aug 2026
Brief summary (registry, in English)
Annually 13000 Norwegians experience an ischemic stroke. The number of stroke is anticipated to increase with 50% within 2030 due to a growing number of elderly. Many of them will have severe function deficits and reduced quality of life. The investigators have established a cohort consisting of 800 patients with first time ischemic stroke treated at hospitals in Central Norway. The investigators want to study the incidence and prognostic markers for death, recurrent stroke and severe functional deficits during a period of 10 years after the initial ischemic stroke. The investigators want to focus on the impact of physical functioning, the level of physical activity and use of medication for secondary prevention on the incidence of death, recurrent stroke and severe functional deficits. The investigators are especially interested in the importance of fulfilling the treatment targets for blood pressure and cholesterol and the importance of smoking cessation in stroke survivors. Our objective is to improve todays stroke treatment and achieve a more efficient use of the health resources in order to increase survival after stroke maintaining a good physical and psychological function and quality of life.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 800 (actual)
- First submitted
- 17 May 2019
- Start date
- 1 May 2015
- Primary completion date
- Aug 2026
- Lead sponsor
- Norwegian University of Science and Technology
- Diseases
- Stroke
- NCT number
- NCT03962127
What you commit to
- Study type: Observational
- Participants enrolled: 800
- From 1 May 2015 to the primary completion date, Aug 2026
- 8 sites 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
- Significant physical disabilities prior to stroke (defined as Modified Rankin ≥5).
Other illness
- Focal neurological symptoms turned out to be not stroke-related
Who the study is looking for
- Cerebral infarction according to ICD-10 CM code I63
- \> 18 years of age
- First time stroke resident in Central-Norway
- Recruited within a time frame of 7 days of hospital admission.
Age in the registry: 18 years to 90 years · Sex: All · Does not accept healthy volunteers
Sites (8)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Ålesund sykehus Coordinator of this site? Confirm its status | Ålesund | Norway | Unknown status |
| Kristiansund Sykehus Coordinator of this site? Confirm its status | Kristiansund | Norway | Unknown status |
| Levanger sykehus Coordinator of this site? Confirm its status | Levanger | Norway | Unknown status |
| Molde Sykehus Coordinator of this site? Confirm its status | Molde | Norway | Unknown status |
| Namsos Sykehus Coordinator of this site? Confirm its status | Namsos | Norway | Unknown status |
| Orkdal Sykehus Coordinator of this site? Confirm its status | Orkanger | Norway | Unknown status |
| St Olavs Hospital Coordinator of this site? Confirm its status | Trondheim | Norway | Unknown status |
| Volda Sykehus Coordinator of this site? Confirm its status | Volda | Norway | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.