Skip to content

The effect of Pentoxifylline on patients with coronary slow flow

Investigating the effect of Pentoxifylline on echocardiography parameters in patients with coronary slow flow

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220516054874N19
Enrollment
48
Registered
2024-08-03
Start date
2024-08-10
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Coronary slow flow syndrome. Other forms of angina pectoris

Interventions

Intervention 1: Intervention group: Patients with slow coronary flow receiving common treatments (including aspirin, statins, beta-blockers and angiotensin-converting enzyme inhibitors) along with Pen

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Diagnosing slow flow of coronary arteries based on angiography results corrected TIMI frame count of more than 27 frames per second Age older than 18 years old Consent to admission to the study

Exclusion criteria

Exclusion criteria: Previous use of pentoxifylline or other methylxanthine drugs Renal dysfunction with GFR < 20 Hepatic dysfunction Body mass index < 18.5 Pregnant or suspected pregnancy

Design outcomes

Primary

MeasureTime frame
Echocardiographic parameters including: Left ventricular ejection fraction, Left Atrial Volume Index, E/e' ratio, diastolic velocities. Timepoint: The beginning of the study and one months later. Method of measurement: Echocardiography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Behzad Senobari

Mashhad University of Medical Sciences

senobarib4001@mums.ac.ir0095 5138012739

Outcome results

None listed

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