Pentoxifylline as an Adjunct Therapy for Patients With Eisenmenger Syndrome: a Randomized Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 10
Maximum Age: 80
Healthy Volunteers: f
View:

• Eisenmenger syndrome in functional class II, III or IV (World Health Organization for Pulmonary Hypertension).

• Using or not oral anticoagulation with warfarin.

Locations
Other Locations
Brazil
Antonio Augusto Barbosa Lopes
RECRUITING
São Paulo
Contact Information
Primary
Antonio Augusto Barbosa Lopes, MD
aablopes@usp.br
+55 11 2661-5409
Backup
Mariana Cappelletti Galante, PharmD
Mariana.galante@hc.fm.usp.br
+55112661-5709
Time Frame
Start Date: 2022-06-03
Estimated Completion Date: 2026-09-30
Participants
Target number of participants: 48
Treatments
No_intervention: No treatment group
24 patients that will continue receiving routine treatment for PAH
Other: Pentoxifylline
24 patients that will receive pentoxifylline and the routine treatment for PAH
Sponsors
Leads: University of Sao Paulo General Hospital
Collaborators: InCor Heart Institute

This content was sourced from clinicaltrials.gov