Actively Recruiting
Clinical Predictors of Short Term Outcomes of Ablation of Idiopathic Monomorphic PVCs
Led by Assiut University · Updated on 2024-07-05
28
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to identify clinical factors that predict short-term outcomes after the ablation treatment of idiopathic monomorphic premature ventricular contractions (PVCs), a type of heart rhythm disorder known as arrhythmia. The study is observational and focuses on understanding which patient characteristics influence treatment results over a two-year period. Participants will undergo a 3D carto-guided ablation procedure to treat their idiopathic monomorphic PVCs. This study observes the effects of this procedure without comparing it to other treatments or placebo. The main focus is on evaluating how different clinical factors relate to the success of the ablation in the short term. During the study, participants will be assessed for clinical predictors of treatment outcomes over two years. Researchers will monitor the heart rhythm and other clinical parameters to understand the procedure's effectiveness for each patient. This includes regular follow-up evaluations to gather data on the ablation's success and any related health changes.
CONDITIONS
Brief Title
Clinical Predictors of Short Term Outcomes of Ablation of Idiopathic Monomorphic PVCs
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with idiopathic monomorphic premature ventricular contractions (PVCs)
You will not qualify if you...
- Patients with heart failure
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single day
Participants undergo ablation of idiopathic monomorphic premature ventricular contractions (PVCs).
1 visit (in-person)
Duration - Up to 2 years
Participants are monitored to assess short term outcomes following ablation.
Follow-up visits as per clinical schedule
Trial Site Locations
Total: 1 location
1
Assiut university
Asyut, Egypt
Actively Recruiting
Research Team
M
Mohammed M Tony
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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