← Eichor
Study identifier: NCT07354607 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effect of Transcutaneous Electrical Stimulation on Peripheral Blood Flow

Condition: Volunteer · Adult  ·  Sponsor: Centre Hospitalier Metropole Savoie

PhaseNA
Planned participants36
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

leo blervaque  ·  +33 4 79 96 59 10  ·  leo.blervaque@ch-metropole-savoie.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Centre Hospitalier Métropole SavoieChambéry, FranceRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07354607