Actively Recruiting

Age: 18Years +
All Genders
ID07317323

Norwegian Spontaneous Coronary Artery Dissection Study (NOR-SCAD Study)

Led by Oslo University Hospital · Updated on 2026-01-05

300

Participants Needed

3

Research Sites

N/A

Total Duration

On this page

Sponsors

O

Oslo University Hospital

Lead Sponsor

U

University Hospital, Akershus

Collaborating Sponsor

AI-Summary

What this Trial Is About

The Norwegian Spontaneous Coronary Artery Dissection Study (NOR-SCAD) is a national, multicenter prospective observational study focused on people aged 18 years or older who are hospitalized with spontaneous coronary artery dissection (SCAD). Researchers are investigating the risk factors, complications, and major adverse cardiac events (MACE) that may occur within the first year after SCAD. The study also aims to evaluate the usefulness of coronary CT angiography (CTA) in diagnosis and follow-up. Participants are enrolled during their initial hospital stay where imaging and blood samples are collected. Follow-up includes scheduled visits at 8 weeks for a control CT scan, at 12 weeks for a thorough physical exam with cardiac assessments, blood tests, and a cardiopulmonary exercise test (CPET). A final phone call at 52 weeks checks for clinical events and collects additional information. During the study, participants undergo coronary CTA scans, cardiac exams, blood sampling, genetic testing, and structured questionnaires to assess quality of life. Researchers track major cardiac events and changes seen in imaging over time. The total follow-up lasts 52 weeks, with the main outcome being the occurrence of major adverse cardiac events during this period.

CONDITIONS

Brief Title

Norwegian Spontaneous Coronary Artery Dissection Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Diagnosed with spontaneous coronary artery dissection (SCAD)
Not Eligible

You will not qualify if you...

  • Severe kidney failure
  • Severe allergic reaction to contrast dye

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - 1 week

Participants undergo acute hospitalization with CT imaging and blood sample collection to confirm SCAD diagnosis and assess initial condition.

1 visit (in-person)

Monitoring

Duration - 12 weeks

Participants receive follow-up coronary CT angiography (CTA) and comprehensive physical and cardiac examinations including blood samples and cardiopulmonary exercise testing to monitor recovery and cardiac health.

2 visits (in-person) at Week 8 and Week 12

Long-term Monitoring

Duration - Approximately 40 weeks

Participants are monitored through a final follow-up phone call to assess clinical events and quality of life outcomes one year after SCAD diagnosis.

1 follow-up phone call at Week 52

Trial Site Locations

Total: 3 locations

1

Haukeland University Hospital

Bergen, Norway

Actively Recruiting

2

Akershus University Hospital

Oslo, Norway

Actively Recruiting

3

Rikshospitalet, Oslo University Hospital

Oslo, Norway

Actively Recruiting

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Research Team

A

Anna Louise Astad Sørlie, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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