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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04891081
Other study ID # 0000
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 1, 2019
Est. completion date June 9, 2021

Study information

Verified date May 2021
Source University Medical Centre Ljubljana
Contact Mojca Jensterle, MD, PhD
Phone 03861 522 35 64
Email mojca.jensterlesever@kclj.si
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The aim of our study is to compare plasma metanephrines in patients with cyanotic and acyanotic congenital heart disease and possible association with chronic hypoxic stress.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date June 9, 2021
Est. primary completion date May 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients with congenital heart disease attending regular follow up Exclusion Criteria: - missing main data in medical documentation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Slovenia Department of Internal Medicine, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia Ljubljana

Sponsors (3)

Lead Sponsor Collaborator
University Medical Centre Ljubljana University of Ljubljana, Faculty of Medicine, University Rehabilitation Institute, Republic of Slovenia

Country where clinical trial is conducted

Slovenia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Plasma metanephrine level Level of plasma metanephrine baseline, one point of time in a cross-sectional study
Primary Plasma normetanephrine level Level of plasma normetanephrine baseline, one point of time in a cross-sectional study
Secondary Hypoxemia Length of hypoxemia presence in years baseline, one point of time in a cross-sectional study
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