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The effect of pentoxifylline on ventricular arrhythmia

Investigating the effect of pentoxifylline on ventricular arrhythmia in heart failure patients with Implantable Cardioverter Defibrillator

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220516054874N16
Enrollment
72
Registered
2024-06-08
Start date
2024-06-04
Completion date
Unknown
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ventricular arrhythmia. Paroxysmal tachycardia

Interventions

Intervention 1: Intervention group: Taking pentoxifylline 400 mg tablets three times a day for 3 months. Intervention 2: Control group: Taking placebo tablets, which look exactly like 400 mg pentoxify

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age older than 18 years old Heart failure diagnosis ICD implantation > 6 months before eligibility test Signed written informed consent to participate in the study

Exclusion criteria

Exclusion criteria: Using Pentoxifylline or other methyl Methylxanthines New York Heart Association Class IV heart failure Renal dysfunction with eGFR < 30 Hepatic dysfunction Body mass index < 18.5 kg/m2 Pregnant or suspected pregnancy Patients with the following events within 3months before the eligibility test: alteration of antiarrhythmic drug, catheter ablation for ventricular arrhythmia, coronary revascularization, open-heart surgery, development of coronary artery disease, stroke or transient ischemic stroke, seizure, infection requiring hospitalization, heart failure requiring hospitalization Other comorbidities including various infections, major surgery, type 1 diabetes, pituitary or adrenal insufficiency, cancer ICDs unable to record cardiac arrhythmias

Design outcomes

Primary

MeasureTime frame
Frequency of the ventricular arrhythmias (PVC, NSVT, VT, VF). Timepoint: The beginning of the study and 3 months later. Method of measurement: ICD (implantable cardioverter-defibrillator) record.

Secondary

MeasureTime frame
Hospitalization. Timepoint: The beginning of the study and 3 months later. Method of measurement: Checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Zahra Zandi

Mashhad University of Medical Sciences

Zandiz@mums.ac.ir0095 5138012739

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026