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Acute and Chronic Pain After One-stage Hybrid Arrhythmia Ablation Surgery

TerminatedNot applicableNCT05211492
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

After one-stage hybrid arrhythmia ablation surgery there are possible side effects like acute and chronic pain. There is a lot of research surrounding these pains but not specifically after one-stage hybrid arrhythmia ablation surgery. The investigators want to research factors that may be associated with the absence of chronic pain after hybrid ablation include ketamine, peroperative opioids, loco-regional blocks, neuraxial blocks, wound infiltration, postoperative patient-controlled analgesia. The presence of corticosteroids or NSAIDS, will also be evaluated. Furthermore, non-adaptable factors such as genetics complicate the onset of chronic post-operative pain. Taking existing knowledge in this field into account, incidence risk as well as acute pain duration and intensity and their effects on chronic pain will become the primary focus of this study. The investigators will contact all patients who had a one-stage hybrid arrhythmia ablation surgery at UZ Brussels. Participants will be sent a questionnaire with a consent form in and a survey asking about their pain 3 months postop and their current pain management therapy.

Study details

Official title
Acute and Chronic Pain After One-stage Hybrid Arrhythmia Ablation Surgery: A Study on the Presence of Chronic Pain After Hybrid Ablation and Factors That May be Associated
Sponsor
Universitair Ziekenhuis Brussel
Start date
2023-02-01
Primary completion
2025-06-01
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Countries
Belgium
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * 18 years of age or older * he/she must understand and read the Dutch, French or English language * be able to digitally agree to participate in the study * had to have a one stage hybrid procedure at least three months ago * have an ASA score of I, II or III. Exclusion Criteria: * Patients with previously known chronic pain syndromes, fibromyalgia, complex regional pain syndrome are excluded. * Subjects with previous known chronic conditions such as diabetes neuropathy, rheumatoid arthri-tis, … are also excluded. * Subject are excluded if they underwent a surgical treatment within the observed period. * Patients are excluded when under treatment with chemotherapy/radiotherapy * Pregnant patients are also excluded. * Patients with known psychological conditions such as depression are excluded.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05211492