Study on Low-Dose Colchicine for Patients with Peripheral Artery Disease to Reduce Cardiovascular Risks

1 1 1

What is this study about?

This clinical trial is focused on studying the effects of a medication called Colchicine in patients with Peripheral Artery Disease (PAD). Peripheral Artery Disease is a condition where the blood vessels outside the heart and brain become narrowed, often leading to reduced blood flow to the limbs. The study will use Colchicine Tiofarma 500 microgram Tablets, which is a low-dose form of the medication, to see if it can help reduce the risk of serious heart and blood vessel problems in people with this condition.

The purpose of the study is to examine how effective and safe Colchicine is in lowering the chances of events like heart attacks, strokes, or severe issues with blood flow to the limbs that might require medical procedures or even amputation. Participants in the study will either receive the Colchicine tablets or a placebo, which looks like the medication but does not contain the active ingredient. The study will last for a period of time, during which participants will take the tablets daily and be monitored for any changes in their health.

Throughout the study, researchers will keep track of various health outcomes, such as the occurrence of heart-related events, hospitalizations, and any need for medical procedures to improve blood flow. The goal is to determine if taking Colchicine can help improve the quality of life and reduce the risk of serious complications for people living with Peripheral Artery Disease.

1 joining the study

Upon joining the study, the patient will be informed about the trial’s purpose and procedures. Written informed consent is required to participate.

2 initial assessment

An initial assessment will be conducted to confirm eligibility. This includes checking for symptoms of peripheral arterial disease, such as intermittent claudication or rest pain, and verifying medical history.

3 medication administration

The patient will receive either Colchicine Tiofarma 500 microgram Tablets or a placebo. The medication is taken orally once daily. The purpose is to evaluate the effectiveness of colchicine in reducing cardiovascular events.

4 regular follow-up visits

Regular follow-up visits will be scheduled to monitor the patient’s health and any side effects. These visits will include assessments of cardiovascular health and limb condition.

5 end of study evaluation

At the end of the study, a final evaluation will be conducted. This will assess the overall impact of the medication on cardiovascular and limb health.

Who Can Join the Study?

  • Must be over 18 years old.
  • Have symptoms of atherosclerotic LE PAD (Peripheral Arterial Disease in the legs) and meet at least one of the following conditions:
    • Experience intermittent claudication, which means pain in the legs during walking, with an ankle/arm blood pressure ratio (ABI) of 0.90 or less, or have an artery that is narrowed by 50% or more. Additionally, must have one of the following:
      • More than one area in the body affected by atherosclerosis (a condition where arteries become narrowed and hardened).
      • Have diabetes.
      • Have heart failure.
      • Have chronic kidney disease with an eGFR (a test that measures kidney function) of less than 60 mL/min/1.73 m².
    • Experience rest pain (pain mostly in the foot), or have necrosis (tissue death) of the limb, or gangrene (severe tissue damage) of the limb, corresponding to specific medical stages. Must also have an ankle/arm blood pressure ratio (ABI) of 0.90 or less, or an artery that is narrowed by 50% or more. If the ankle arteries cannot be compressed, a toe pressure of 60 mm Hg or less, or a toe-brachial index of 0.70 or less, is acceptable.
    • Have undergone revascularization, which is a procedure to restore blood flow, such as limb bypass surgery or other procedures to open up blocked arteries.
    • Have had a leg or foot amputation due to problems with blood flow in the arteries.
  • Must provide written informed consent, meaning they agree to participate in the study after being fully informed about it.

Who Cannot Join the Study?

  • Patients who do not have peripheral arterial disease cannot participate. This is a condition where the blood vessels outside the heart and brain become narrowed or blocked.
  • Patients who are not within the specified age range cannot participate. The age range includes adults and older adults.
  • Patients who are part of a vulnerable population cannot participate. This means people who might need special protection or care.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
University Hospital Maastricht Maastricht The Netherlands
Katholieke Universiteit te Leuven Leuven Belgium

Other Sites

Site Name City Country Status
Groene Hart Ziekenhuis Gouda The Netherlands
Jeroen Bosch Ziekenhuis Stichting s-Hertogenbosch The Netherlands
Alrijne Zorggroep Stichting Leiderdorp The Netherlands
Azienda Unita’ Locale Socio Sanitaria N. 2 Marca Trevigiana Treviso Italy
Azienda Ospedaliera di Padova Padua Italy
Università degli studi Gabriele D’Annunzio Chieti-Pescara Centro di Studi e tecnologie avanzate Chieti Italy
Universitair Medisch Centrum Utrecht Utrecht The Netherlands
Meander Medical Center Amersfoort The Netherlands
Deventer Ziekenhuis Deventer The Netherlands
Slingeland Ziekenhuis Doetinchem The Netherlands
Azienda Ulss 6 Euganea Padua Italy
Ueurmnukowxugvoyddyzd Eordz Asa Essen Germany
Uandgajjadok Mjjsqnz Cqwerry Gpmjlvcxv Groningen The Netherlands
Oybtufzn Sfm Gviadrop E Pzpkq Venice Italy
Azvvzrk Uwidb Lpbchl Siipn Subwozfoq Nk 1 Diujbufw Belluno Italy
Atgup 5 Purqxvfzo Pnertjme Oordphqjstw Dj Ryucoz Rovigo Italy
Ssk Ekmfywhlh Hbjoxqzi Twjvobb Tilburg The Netherlands

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Belgium Belgium
Recruiting
30.11.2024
Germany Germany
Not yet recruiting
30.11.2024
Italy Italy
Not yet recruiting
30.11.2024
The Netherlands The Netherlands
Recruiting
30.11.2024

Trial locations

Investigated drugs:

Colchicine is a medication being studied in this trial for its potential to reduce the risk of serious cardiovascular events. These events include heart attacks, strokes, and severe problems with blood flow in the limbs that might require surgery. The trial is focused on patients with peripheral artery disease, a condition that affects blood flow in the arteries. The goal is to see if colchicine can help lower the chances of these serious health issues.

Peripheral Arterial Disease – This condition involves the narrowing or blockage of the arteries, primarily affecting the legs. It occurs when fatty deposits build up on the walls of the arteries, reducing blood flow to the limbs. As the disease progresses, individuals may experience pain or cramping in the legs or hips, especially during physical activities like walking or climbing stairs. Over time, the symptoms can worsen, leading to more severe pain even at rest. In advanced stages, the reduced blood flow can cause wounds or sores on the feet or legs that heal slowly or not at all. If left unchecked, it can lead to critical limb ischemia, where the lack of blood flow becomes a serious concern.

Trial ID:
2024-512091-35-01
NCT ID:
NCT04774159
Trial Phase:
Therapeutic confirmatory (Phase III)

Other Trials to Consider

  • A study to evaluate the efficacy and safety of orforglipron in patients with peripheral artery disease

    Recruiting

    1 1
    France The Netherlands Poland Slovakia
  • Study of APAC (antiplatelet, anticoagulant) treatment in patients with peripheral arterial disease and chronic limb-threatening ischemia during blood vessel restoration procedure

    Recruiting

    1 1 1
    Investigated diseases:
    Finland