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RecruitingNCT07771335ESProUpdated Oct 2, 2026

The Erlanger Stroke Registry (ESPro) is the Only Ongoing Prospective Population-based Stroke Registry in Germany, Started in 1994. ESPro Includes All Hospitalized and Non-hospitalized Patients With Stroke in the Community of Erlangen (120.000 Inhabitants), With a Long-life Follow-up.

An observational study in Intracerebral Haemorrhage (ICH), Cerebral Infarction and Cerebral Infarction Due to Thrombosis of Cerebral Arteries, sponsored by University of Erlangen-Nürnberg Medical School. Recruiting at 3 sites in Germany. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-02.

Sponsored by University of Erlangen-Nürnberg Medical School · Observational

From the registry’s dates

  • Started Apr 1994; still recruiting 32 years 7 months later.
Updated Oct 2, 2026Title changedGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
17,000
Ages
18 Years and older
Sex
All
01

Study summary

Stroke is a disease that primarily affects older adults and, with an estimated 64,000 deaths in 2024, is one of the leading causes of death in Germany. Estimates of its prevalence and the burden of disease within the German population are therefore essential for calculating future healthcare needs and guide health policy planning. When the first stroke units (SU) began to emerge in Germany in 1994, health insurers raised the question of the total number of stroke patients requiring care. Unfortunately, at that time there were no reliable figures available to determine the nationwide need for stroke units. This marked the birth of the Erlangen Stroke Registry (ESPro).

For 32 years (1994-2026), ESPro has been continuously collecting data on the epidemiology, clinical course, and care of stroke and dementia, two of the most common diseases. The ESPro is designed as a regional, population-based registry that includes, as far as possible, all diagnosed strokes-that is, both hospitalized and non-hospitalized patients-regardless of age group or severity of the condition. Patients enrolled in the city of Erlangen undergo close monitoring of their clinical course and are followed up at intervals of 3 and 12 months, and then annually for the rest of their lives. This long-term follow-up enables comprehensive health services research on stroke, a widespread disease. Direct information on the course of the disease, its treatment, and care can be gleaned from registry data and incorporated into preventive medicine, treatment, and care planning.

02

Conditions studied

  • Intracerebral Haemorrhage (ICH)
  • Cerebral Infarction
  • Cerebral Infarction Due to Thrombosis of Cerebral Arteries
  • Cerebral Infarction Due to Embolism of Cerebral Arteries
  • Stroke, Not Specified as Haemorrhage or Infarction
  • Transient Cerebral Ischaemic Attacks and Related Syndromes
  • Vascular Dementia (VaD)
  • Multi-infarct Dementia
  • Cerebral Vein Thrombosis

Keywords

  • Stroke
  • Erlangen
  • Germany
  • Registry
03

In context

Cerebral Hemorrhage

457 studies on the registry are indexed under Cerebral Hemorrhage; 172 are open to participants now.

This study's planned enrollment of 17,000 is above the median of 300 across 180 observational studies indexed under Cerebral Hemorrhage.

Browse Cerebral Hemorrhage studies →

Lead sponsor

University of Erlangen-Nürnberg Medical School is the lead sponsor of 276 studies on the registry; 52 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The Erlangen Stroke Project (ESPro) is a community-based survey of all cases of stroke occurring in a university town, located in Bavaria in Southeast Germany. Several overlapping sources of information were used to ensure complete case ascertainment: (1) hospital admission and discharge lists and computer-linked records systems; (2) regular checks of all relevant hospital wards and residential and nursing homes; (3) records of ambulance and emergency services; (4) GPs; and (5) death certificates.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • All cases of stroke defined according to WHO criteria, as "rapidly developing clinical symptoms and/or signs of focal, and at times global, loss of cerebral function, with symptoms lasting more than 24 hours or leading to death, with no apparent cause other than that of vascular origin occurring in Erlangen, Bavaria
  • No restrictions regarding age (provided they are of legal age), socioeconomic circumstance, stroke severity, or prior health status

Exclusion criteria

Exclusion Criteria:

  • Patients with transient episodes lasting less than 24 hours and those with asymptomatic lesions detected by brain imaging ("silent infarcts")
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
17,000 participants (estimated)
Target follow-up
30 Years
Patient registry
Yes

Groups and cohorts

  • People with stroke

    All individuals diagnosed with stroke (both hospitalized and non-hospitalized)

06

What researchers measure

Primary outcomes

  1. Name

    Time frame: Baseline

  2. Address

    Time frame: Baseline

  3. Postal code

    Time frame: Baseline

  4. Telephone number

    Time frame: Baseline

  5. Gender

    Time frame: Baseline

  6. Date of birth

    as date

    Time frame: Baseline

  7. Date of death

    as date

    Time frame: After 3 months, after 12 months, then annually until the event occurs. Currently there is a follow-up of 32 years-up

  8. Nationality

    Time frame: Baseline

  9. Education

    Time frame: Baseline

  10. Employment status

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  11. Marital status

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  12. Number of children

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  13. Name of the health insurance company

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  14. Length of residence in the study area

    Time frame: Baseline

  15. Living arrangements

    Which kind of living arrangement (own home environment, assisted living, nursing home) and who are the people, who live in this arrangement (alone, spouse, children, relatives, others)

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  16. Telephone number of the General practitioner

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  17. Assistance

    yes/ no

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  18. Name of the contact person

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  19. Telephone number of the contact person

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  20. Relationship between the patient and the contact person

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  21. National Institutes of Health Stroke Scale (NIHSS)

    Total Score Range: 0-42 (15 items, each scored on 3-5 point ordinal grades, 0 = normal), higher values indicate greater stroke severity (0 = no stroke symptoms, 1-4 minor, 5-15 moderate, 16-20 moderate-to-severe, 21-42 severe)

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  22. (Modified) Rankin Scale

    Total Score Range: 0-6 (7-point ordinal disability scale), higher values indicate worse (higher) disability (0 = no symptoms, 1 = no significant disability, 2 = slight disability, 3 = moderate disability, 4 = moderately severe disability, 5 = severe disability, 6 = death)

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  23. Mini-Mental State Examination (MMSE)

    Total Score Range: 0-30, higher values indicate better cognitive performance

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  24. Medication

    Name of the drug

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  25. Medication

    Quantity

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  26. Medication

    Dose in milligrams per day

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  27. Charlson Comorbidity Index (CCI)

    Total Score Range: 0-33, higher values indicate a worse (greater) comorbid disease burden

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  28. Hypertension

    yes/ no

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  29. Diabetes mellitus

    yes/ no

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  30. Hypercholesterinemia

    yes/ no

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  31. TOAST-Classification

    Categorical etiologic classification system; it sorts ischemic stroke into 5 mutually exclusive subtype categories: (1) large-artery atherosclerosis, (2) cardioembolism, (3) small-vessel occlusion (lacunar), (4) stroke of other determined etiology, and (5) stroke of undetermined etiology

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  32. Medical Outcomes Study Social Support Survey (MOS-SSS)

    Total Score Range: Raw sum score: 19-95 (19 items, each rated on the 5-point frequency scale: 1 = none of the time … 5 = all of the time), Transformed index (0-100 scale), higher values indicate better (greater) perceived/available social support

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  33. Short Form 36 Health Survey (SF-36)

    Physical health and mental health summary scores, Total Score Range: 0-100, norm-based scoring, higher values indicate a better physical/mental health status

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  34. Barthel Index

    Total Score Range: 0-100, higher values indicate better functional independence (less disability)

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  35. Frenchay Activities Index (FAI)

    Total Score Range: 15-60, higher values indicate better (greater) frequency/independence in instrumental activities of daily living (IADL)

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

  36. Functional Independence Measure (FIM)

    Total Score Range: 18-126, Subscales: FIM-motor 13-91, FIM-cognitive 5-35, higher values indicate better (greater) functional independence (18 = total dependence, 126 = total independence)

    Time frame: Baseline, after 3 months, after 12 months, then annually until the end of the study. Currently there is a follow-up of 32 years

07

Study locations

3 of 3 sites recruiting
  • Malteser Waldkrankenhaus St. Marien
    Erlangen, 91054, Germany
    Recruiting
  • Universitätsklinikum Erlangen
    Erlangen, 91054, Germany
    Recruiting
  • Klinikum am Europakanal
    Erlangen, 91056, Germany
    Recruiting
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: Yes — Information on the use of research data from the Erlangen Stroke Registry can be found on the website at the following link: https://www.izph.fau.de/projekte/erlanger-schlaganfallregister/#angebot-zur-nutzung-von-forschungsdaten-aus-dem-erlanger-schlaganfallregister

09

Updates

1 registry update since Sep 25, 2026
Title
The Erlanger Stroke ProjectRegistry (ESPro) is anthe Only Ongoing Prospective Population-based Stroke Registry in Germany, IncludingStarted in 1994. ESPro Includes All Hospitalized and NonhospitalizedNon-hospitalized Patients With Stroke in the CityCommunity of Erlangen (120.000 Inhabitants), With a Long-life Follow-up.
Oct 2, 2026
Show all 1 update
  1. Oct 2, 2026
    Title The Erlanger Stroke ProjectRegistry (ESPro) is anthe Only Ongoing Prospective Population-based Stroke Registry in Germany, IncludingStarted in 1994. ESPro Includes All Hospitalized and NonhospitalizedNon-hospitalized Patients With Stroke in the CityCommunity of Erlangen (120.000 Inhabitants), With a Long-life Follow-up.
    + 1 other change: design details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07771335
Responsible party
Sponsor
First posted
Aug 18, 2026
Start date
Apr 1, 1994
Primary completion
Mar 30, 2094 (estimated)
Completion
Mar 30, 2094 (estimated)
Last update
Oct 2, 2026

Study contacts

Peter L. Kolominsky-Rabas, Univ.-Prof. Dr. med.
Contact
peter.kolominsky-rabas@fau.de
+49 9131 85-35855

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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