Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07354607

Effect of Transcutaneous Electrical Stimulation on Peripheral Blood Flow

Led by Centre Hospitalier Metropole Savoie · Updated on 2026-03-10

36

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

Sponsors

C

Centre Hospitalier Metropole Savoie

Lead Sponsor

L

Laboratoire Interuniversitaire de Biologie de la Motricité

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if transcutaneous electrical nerve stimulation can affect blood flow in healthy volunteers. The main question it aims to answer is: Determine the stimulation parameters (frequency in the range 5- 100Hz and proximal or distal placement) inducing the most significant hyperaemic response in volunteers. Participants will attend to one visit ( 1h30) , 6 protocol of stimulation will be tested on his arm . If his agree, an optionnal measure will be made during another visit. During this optionnal visit, two modalities of intensity adjustment will be tested in regard of the result of the first part of the study.

CONDITIONS

Official Title

Effect of Transcutaneous Electrical Stimulation on Peripheral Blood Flow

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Subject aged 18 years or older
  • Having freely given written consent, after being informed of the purpose of the study, its conduct and its risks
  • Affiliated with a social security scheme
Not Eligible

You will not qualify if you...

  • Persons with pacemakers or any other implantable electrical devices
  • Pregnant women
  • Suffering from dermatological conditions or muscle/skin lesions on the arms and forearms
  • Participant unable to give free and informed consent
  • Participant unable to comply with the specific procedures of the study
  • Participant deprived of liberty or benefiting from legal protection measures

AI-Screening

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Trial Site Locations

Total: 1 location

1

Centre Hospitalier Métropole Savoie

Chambéry, France, 73000

Actively Recruiting

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Research Team

L

leo blervaque

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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