Actively Recruiting

Phase 2
Age: 40Years - 90Years
All Genders
NCT06420752

Passive Stretching in Peripheral Arterial Disease Patients

Led by University of Wisconsin, La Crosse · Updated on 2025-04-02

64

Participants Needed

1

Research Sites

293 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Peripheral artery disease (PAD) leads to higher mortality rates and strains healthcare systems due to increased costs. It causes leg pain during walking due to reduced blood flow. Nitric oxide (NO) deficiency contributes to vascular issues in PAD, with few effective treatments available. Passive calf muscle stretching boosts NO levels, vascular health, and walking ability in PAD patients. However, the inflammatory processes underlying these improvements are unclear. This study aims to track inflammatory markers and cardiovascular changes during 12 weeks of passive stretching. Additionally, combining stretching with dietary nitrate could further enhance walking capacity by reducing reactive oxygen species. The study will monitor inflammation, vascular function, and oxidative capacity to understand the effects on functional ability in PAD patients. This research is crucial for improving physical function and addressing exercise intolerance in PAD.

CONDITIONS

Official Title

Passive Stretching in Peripheral Arterial Disease Patients

Who Can Participate

Age: 40Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ankle-brachial index of 0.90 or less
  • Stable condition for at least 3 months
  • Age between 40 and 90 years
Not Eligible

You will not qualify if you...

  • Habitual exercise or cardiovascular rehabilitation program during the past 3 months
  • Critical limb ischemia, amputation, or leg pain at rest
  • Major surgery or lower extremity revascularization in the last 3 months
  • Heart failure
  • Kidney disease
  • Beet allergy
  • Crohn's disease
  • Current smoker

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Wisconsin La Crosse

La Crosse, Wisconsin, United States, 54650

Actively Recruiting

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Research Team

J

Jacob T Caldwell, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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