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Flavonoid

MPFF for Post-Thrombotic Syndrome (MUFFIN-PTS Trial)

Phase 3
Waitlist Available
Led By Susan R Kahn, MD, MSc
Research Sponsored by Sir Mortimer B. Davis - Jewish General Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Females of childbearing age must use medically approved method of birth control and must have negative pregnancy test results at the time of randomization
Villalta score ≥5 with at least two of the following four PTS manifestations (daily heaviness, cramps, pain, and objective edema) in the leg ipsilateral to a previous objectively diagnosed DVT, or DVT of unknown date but with presence of residual proximal or distal venous obstruction on ultrasound
Must not have
Age<18 years
Liver cirrhosis Child-Pugh class C
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3, 6, 9 months
Awards & highlights

Summary

This trial tests if a pill made from purified plant compounds can help people with chronic leg vein issues after a blood clot. The goal is to see if it improves their symptoms and quality of life by making their veins work better and reducing swelling. Micronized purified flavonoid fraction (MPFF) has been studied for its effectiveness in improving symptoms and quality of life in patients with chronic venous disease.

Who is the study for?
The MUFFIN-PTS Trial is for individuals with Post-Thrombotic Syndrome who experience symptoms like heaviness, cramps, pain, and leg swelling. Participants must be adults not on venoactive drugs recently, without severe liver or kidney disease, not pregnant or breastfeeding, and able to consent.
What is being tested?
This trial tests if taking Micronized Purified Flavonoid Fraction (MPFF) daily for six months can improve symptoms and quality of life in Post-Thrombotic Syndrome patients compared to a placebo.
What are the potential side effects?
Potential side effects of MPFF are generally mild but may include gastrointestinal discomfort such as upset stomach or diarrhea. Allergic reactions could occur in those sensitive to flavonoids.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am using birth control and my pregnancy test was negative.
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I have a Villalta score of 5 or more and experience daily heaviness, cramps, pain, or swelling in one leg due to a past blood clot.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I am under 18 years old.
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My liver condition is severe (Child-Pugh class C).
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I have changes in my mental status, either suddenly or over time.
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I am currently hospitalized.
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I have severe kidney disease and may be on dialysis.
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I have an open sore on the same side as my vein problem.
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I cannot speak English or French.
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I have had a blood clot in my leg within the last 3 months.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3, 6, 9 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3, 6, 9 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Secondary study objectives
Change in PTS
Cramps
General Quality of life
+16 more

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: VenixxaActive Control1 Intervention
Micronized Purified Flavonoid Fraction (MPFF) for 6 months MPFF 500 mg, BID (morning and evening) for 6 months
Group II: PlaceboPlacebo Group1 Intervention
Placebo for 6 months 1 Tablet, BID (morning and evening) for 6 months

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Post-Thrombotic Syndrome (PTS) aim to improve venous function, reduce inflammation, and enhance lymphatic drainage. Micronized Purified Flavonoid Fraction (MPFF) is thought to improve venous tone, reduce inflammation, and enhance lymphatic drainage, which may alleviate symptoms of PTS and improve quality of life (QOL). These mechanisms are crucial for PTS patients as they help reduce pain, swelling, and other debilitating symptoms, thereby enhancing overall mobility and daily functioning.
The effect of exogenous phosphocreatine on maximal walking distance, blood rheology, platelet aggregation, and fibrinolysis in patients with intermittent claudication.Role of platelet-activating factor (PAF) in platelet accumulation in rabbit skin: effect of the novel long-acting PAF antagonist, UK-74,505.Alterations in platelet function in patients receiving interleukin-6 as cytokine therapy.

Find a Location

Who is running the clinical trial?

Sir Mortimer B. Davis - Jewish General HospitalLead Sponsor
58 Previous Clinical Trials
21,128 Total Patients Enrolled
Susan R Kahn, MD, MScPrincipal InvestigatorJewish General Hospital (Montreal, Quebec, Canada)
Jean-Philippe Galanaud, MD, PhDPrincipal InvestigatorSunnybrook Health Sciences Centre, Toronto, Ontario, Canada
1 Previous Clinical Trials
1,300 Total Patients Enrolled

Media Library

Micronized Purified Flavonoid Fraction (Flavonoid) Clinical Trial Eligibility Overview. Trial Name: NCT03833024 — Phase 3
Post-Thrombotic Syndrome Research Study Groups: Venixxa, Placebo
Post-Thrombotic Syndrome Clinical Trial 2023: Micronized Purified Flavonoid Fraction Highlights & Side Effects. Trial Name: NCT03833024 — Phase 3
Micronized Purified Flavonoid Fraction (Flavonoid) 2023 Treatment Timeline for Medical Study. Trial Name: NCT03833024 — Phase 3
~25 spots leftby Sep 2025