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Tight stockings under the microscope: new data on vein pressure

NCT ID NCT01558024

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at how compression stockings of different strengths change the size and pressure of leg veins in people with chronic venous insufficiency and healthy volunteers. Researchers measured vein diameter and leg pressure while participants stood, sat, or lay down. The goal was to better understand how stockings work, not to test a new treatment.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

111 people

The number who actually took part.

Start date

Jul 2014

Finished

Mar 2016

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * The participant must have given his/her informed and signed consent * The participant must be insured or beneficiary of a health insurance plan Inclusion criteria for patients in the venous insufficiency group: * CEAP (Clinical-Etiology-Anatomy-Pathophysiology) Classification : C1S, C3 or C5 Inclusion criteria for healthy volunteers * general good health * subgroups including: * sedentary volunteers (\< 2hours of physical activity per week) * active volunteers (between 2 and 6 hours of physical activity per week) * athletic volunteers (over 6 hours of physical activity per week for at least 1 year) Exclusion Criteria: * The participant is participating in another study, except the "volumetric" counterpart to the present study * The participant is in an exclusion period determined by a previous study * The participant is under judicial protection, under tutorship or curatorship * The participant refuses to sign the consent * It is impossible to correctly inform the participant * The participant is pregnant, parturient, or breastfeeding * Arterial vascular disease, heart, lymph, renal, hepatic, oncologic, metabolic or endocrine or any other condition that may cause or exaggerate edema Exclusion criteria for healthy volunteers: * Risk for abnormal bleeding (hemophilia, anticoagulation or antiplatelet) * Taking diuretics or corticoids

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • CHU de Montpellier - Hôpital Saint-Eloi

    Montpellier, 34295, France

  • CHU de Nîmes - Hôpital Universitaire Carémeau

    Nîmes, 30029, France

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