Actively Recruiting

Age: 18Years - 90Years
All Genders
NCT06223217

Development and Validation of the Modified Version of VascuQol Scale in Patients With Lower Extremity Peripheral Arterial Disease.

Led by RenJi Hospital · Updated on 2024-01-25

480

Participants Needed

1

Research Sites

169 weeks

Total Duration

On this page

Sponsors

R

RenJi Hospital

Lead Sponsor

L

Liyuan Hospital of Tongji Medical College, Huazhong University of Science and Technology

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to assess the utility of the Modified version of VascuQol Scale as an effective biopsychosocial assessment tool for patients suffering from lower extremity peripheral arterial disease.

CONDITIONS

Official Title

Development and Validation of the Modified Version of VascuQol Scale in Patients With Lower Extremity Peripheral Arterial Disease.

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female aged 18-90
  • Diagnosed with lower extremity peripheral arterial disease
  • Willing to comply with specified follow-up evaluations
  • Understands the study nature and provides written informed consent
  • Guidewire has crossed the target lesion before enrollment
  • No restriction on Rutherford, TASC, or GLASS grading
Not Eligible

You will not qualify if you...

  • Pregnant women or females with potential for childbearing
  • Currently participating in another investigational drug or device study without primary endpoint reached
  • Unwilling or refusing to sign informed consent
  • Having other serious diseases affecting quality of life or life expectancy less than 2 years, such as tumors, severe liver disease, or cardiac insufficiency

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

Renji Hospital

Shanghai, Shanghai Municipality, China

Actively Recruiting

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Research Team

J

Jingpu Zhu

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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