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Clinical Trials/NCT05882136
NCT05882136
Completed
Not Applicable

Assessment of the Structure and Function of Heart and Selected Cardiovascular Risk Factors in Patients With Acute Intermittent Porphyria

National Institute of Cardiology, Warsaw, Poland2 sites in 1 country180 target enrollmentApril 5, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Porphyrias, Hepatic
Sponsor
National Institute of Cardiology, Warsaw, Poland
Enrollment
180
Locations
2
Primary Endpoint
Rate of cardiac arrhythmias.
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

This study aims to assess the changes in the cardiovascular system in patients with acute intermittent porphyria (AIP).

Detailed Description

Porphyrias are heterogeneous group of the disorders of heme biosynthesis. Acute intermittent porphyria (AIP) is the most common acute hepatic porphyria, caused by the mutations in the gene encoding hydroxymethylbilane synthase. Clinical symptoms i.e. abdominal pain, nausea, vomiting, paresis or paralysis, coma and/or mental abnormalities may be induced by many porphyrinogenic factors, such as drugs, alcohol, starvation or stress. The symptoms are often accompanied by tachycardia and elevated blood pressure. Due to the non-specific clinical picture, AIP is often diagnosed too late and causes a threat to the patients' lives. There is a scarcity of data regarding the changes in cardiovascular system in patients with AIP. The aim of this study is to assess the structure and function of heart in patients with this disease. The prevalence of hypertension, cardiac arrhythmias and selected cardiovascular risk factors in patients with AIP will also be evaluated. This is a case-control study with prospective observation of the subgroup of patients examined during the exacerbations of AIP. Specific goals: * assessment of the cardiac morphology and function, * assessment of the concentrations of markers of myocardial injury (troponin T) and heart failure (NT-proBNP), * assessment of the prevalence of cardiac arrhythmias and electrocardiographic abnormalities, * assessment of the blood pressure profiles, * assessment of selected cardiovascular risk factors, * assessment of quality of life, * assessment of clinical and biochemical factors associated with the pathological findings in patients with AIP.

Registry
clinicaltrials.gov
Start Date
April 5, 2019
End Date
February 28, 2024
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
National Institute of Cardiology, Warsaw, Poland
Responsible Party
Principal Investigator
Principal Investigator

Krzysztof Jaworski

Principal Investigator

National Institute of Cardiology, Warsaw, Poland

Eligibility Criteria

Inclusion Criteria

  • acute intermittent porphyria (AIP),
  • age 18-65 years,
  • at least one hospitalization due to exacerbation of AIP.

Exclusion Criteria

  • previous myocardial infarction,
  • heart failure of established (other than porphyria) etiology,
  • severe heart valve disease,
  • congenital heart defects,
  • history of myocarditis,
  • pacemaker,
  • hyperthyroidism / hypothyroidism (except for adequate thyroid hormone replacement therapy),
  • chronic advanced lung diseases,
  • lack of consent to participate in the study.

Outcomes

Primary Outcomes

Rate of cardiac arrhythmias.

Time Frame: day 1 and up to 2 years in case of the exacerbation of AIP

Cardiac arrhythmias observed in 24-hour ECG monitoring.

Number of participants with hypertension.

Time Frame: day 1 and up to 2 years in case of the exacerbation of AIP

Arterial hypertension diagnosed by ambulatory 24-hour blood pressure monitoring.

Number of participants with heart failure and left ventricular dysfunction.

Time Frame: day 1 and up to 2 years in case of the exacerbation of AIP

Heart failure and left ventricular dysfunction assessed by symptoms and echocardiography.

Secondary Outcomes

  • Number of participants with dyslipidemia.(day 1)
  • Number of participants with increased concentrations of markers of heart failure.(day 1 and up to 2 years in case of the exacerbation of AIP)
  • Number of participants with chronic kidney disease.(day 1 and up to 2 years in case of the exacerbation of AIP)
  • Number of participants with increased concentrations of markers of myocardial injury.(day 1 and up to 2 years in case of the exacerbation of AIP)
  • Number of participants with diabetes.(day 1)
  • Level of quality of life.(day 1)

Study Sites (2)

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