Pentoxifylline as an Adjunct Therapy for Patients With Eisenmenger Syndrome

StatusUnknown
PhaseNot applicable
Started

Record status This record was last updated December 15, 2023 (before its estimated September 30, 2024 completion). Its status may not reflect the trial's current state.

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Record History

  1. Minor Changed Registry marked status Unknown (sponsor has not verified the record since Dec 2023); last known: Recruiting
  2. Minor Re-verified, no change to tracked fieldsv2
  3. Minor Study First Submitted
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The Eisenmenger syndrome corresponds to the most advanced form of pulmonary arterial hypertension associated with congenital heart disease. The syndrome causes chronic hypoxemia, with an increase in erythrocyte mass, which predisposes to thrombotic complications. Pentoxifylline is a xanthine derivative and it is considered as a hemorrheological agent with described effects of reduction in erythrocyte and platelet aggregation, adhesion and activation of leukocytes, and endothelial damage. The main objective of this study is to verify if the chronic oral administration of pentoxifylline to Eisenmenger patients induces an increase in the circulating levels of thrombomodulin, a naturally occurring proteoglycan with anticoagulant, anti thrombotic and anti-inflammatory properties.
Trial Details
NCT Number NCT05611268
Lead Sponsor University of Sao Paulo General Hospital
Collaborators: InCor Heart Institute
Conditions
(from sponsor)
Eisenmenger Syndrome
Related terms Eisenmenger Complex, Heart Defects, Congenital, Hypertension, Pulmonary, Thrombosis
Enrollment 48 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov