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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02318498
Other study ID # 2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 2014
Est. completion date April 2019

Study information

Verified date September 2019
Source Karolinska Institutet
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Myocardial infarction with angiographically normal coronary arteries (MINCA) is common (7-8 % of all myocardial infarctions). There are several different causes behind MINCA where "true infarction" due to thromboembolism, myocarditis or Takotsubo stress cardiomyopathy are the main findings. The underlying diagnosis is often made by clinical findings sometimes with the help of cardiac MRI (CMR). Investigators have previously shown that it was possible to give 50 % of the patients a diagnosis made by the combination of clinical findings and CMR made in median 12 days after the acute event. The present study aim at improve the diagnostic accuracy by an early CMR with latest technique.


Description:

The present study aim at improve the diagnostic accuracy in MINCA with an CMR made 2-4 days after the acute event. The aim is to give 70 % of all patients with MINCA (35-70 years old) a definitive diagnosis made by CMR only. One-hundred and fifty patients will be included and compared with a similar historical sample where 50 % of the patients received a diagnosis made by a late CMR and clinical findings. The study has 80 % power to detect this 20 % absolute difference (p <0.05).


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date April 2019
Est. primary completion date November 2018
Accepts healthy volunteers No
Gender All
Age group 35 Years to 69 Years
Eligibility Inclusion Criteria:

- 35-70 years

- Fullfill the diagnosic criteria of myocardial infarction

- Normal coronary angiography or minor atheromatosis

- Sinus rythm on ECG at admission

Exclusion Criteria:

- Previous myocardial infarction

- Known cardiomyopathy

- Pacemaker or claustrophobia

- Severe chronic obstructive lung or kidney disease

- Pulmonary embolism

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
CMR
Intervention performed 2-4 days after admission to hospital with the latest CMR technique including sensitive oedema sequences using T1 mapping

Locations

Country Name City State
Sweden Karolinska Institutet Stockholm

Sponsors (2)

Lead Sponsor Collaborator
Karolinska Institutet Swedish Medical Research Council

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnostic accuracy of an early CMR with the latest technique Show that the more patients get a definite diagnosis (70%) when compared to a historical sample (50%) 2-4 days after admission
Secondary Number of patients with correct diagnosis with echocardiography To study the accuracy of echocardiography compared to CMR using ROC 12 months
Secondary Number of patients with a postive CT angiography and infarction on CMR To study CT angiography findings in relation to myocardial infarction shown by CMR 1 month
Secondary Describe QoL over time 12 months
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