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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05201989
Other study ID # 276727
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 10, 2022
Est. completion date December 10, 2023

Study information

Verified date April 2024
Source Region Örebro County
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Atrial fibrillation (AF) is the most common sustained arrhythmia and the number of patients with AF is expected to increase substantially in the coming decades. One third of patients with AF report no AF-associated symptoms, but up to one-fourth report severe symptoms. It is unclear why patients' experience of AF-related symptoms varies so much. We have previously shown that patients with symptomatic AF exhibit lower pain tolerance than patients with asymptomatic AF, as well as impaired pain inhibitory control and facilitated summation of pain, indicating that pain sensitisation may be of importance in symptomatic AF. In patients with chronic pain conditions, several biomarkers and epigenetic markers associated with generation and /or maintenance of chronic pain have been identified. Previous research of biomarkers and epigenetic markers associated with pain is sparse in patients with AF. The objective is to study levels of biomarkers and epigenetic markers in blood in patients with symptomatic paroxysmal AF (n=100), in relation to severity of AF symptoms, and compared to age- and sex-matched controls without AF (n=100). Blood will be obtained before and after AF ablation and levels of biomarkers, epigenetic markers and cardiac and inflammatory markers, analysed. Patients will complete an AF-specific symptom and a generic health-related quality of life questionnaire. In the future, biomarkers and epigenetic markers associated with pain may be used as a tool for evaluation of patients with AF and have an impact on individualized management. Another possibility is a rationale for future studies of novel analgesics that neutralize biomarkers or antagonizes its receptors.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date December 10, 2023
Est. primary completion date December 10, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria: - On waiting list for AF ablation (only symptomatic subjects are offered ablation) - Paroxysmal AF and persistent AF (AF that is continuously sustained beyond 7 days, including episodes terminated by cardioversion after =7 days) - Written informed consent Exclusion Criteria: - Previous pulmonary vein isolation - Cognitive or psychiatric condition - Diabetes mellitus - Ischemic heart disease - Heart failure - Asthma - Pregnancy - Previous/current drug or alcohol abuse - Previous neurological or concomitant musculoskeletal disorders - Continuous analgesic medication

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Sweden Department of cardiology Örebro

Sponsors (2)

Lead Sponsor Collaborator
Region Örebro County Aalborg University

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Biomarkers and epigenetic markers associated with pain Blood tests will be obtained from subjects the day before, and the day after a planned AF ablation. A total of 30 ml of blood will be obtained at each occasion. The samples will be studied for the association of biomarkers and epigenetic markers to the severity of AF symptoms. Blood samples will be obtained from participants without AF (controls). Biomarkers and epigenetic markers will be compared between the control group and the group with symptomatic AF. 3 days
Secondary Correlation of age, sex, AF duration, health-related quality of life to biomarkers and epigenetic markers. 1 day
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