Tight socks for better sleep? study tests stockings against apnea

NCT ID NCT05477719

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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 Results may not be published yet.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

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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This status has not been confirmed recently, so it may be out of date.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 whether wearing compression stockings during the day for 28 days could reduce the number of breathing pauses (apneas) per hour in people with moderate to severe sleep apnea. The idea is that stockings prevent fluid from building up in the legs and moving to the neck during sleep, which can block breathing. 25 adults who had stopped other apnea treatments or never tried them participated.

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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

25 people

The number who actually took part.

Started

Sep 2022

Finished

Mar 2024

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

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: * patient with moderate to severe sleep apnea-hypopnea syndrome confirmed by polysomnography dating less than 3 months with an index of apneas/hypopneas ≥ 15 apneas-hypopneas/h 1. having been previously treated with nasal ventilation by continuous positive airway pressure and mandibular orthosis and having stopped treatment for at least 10 days, regardless of the duration of use of these two treatments 2. or never treated for their sleep apnea-hypopnea syndrome satisfying the following 3 criteria 1. having 1 or 2 of the following signs daytime sleepiness, severe and daily snoring, feelings of suffocation or suffocation during sleep, daytime fatigue, nocturia, morning headaches. 2. absence of serious cardiovascular or respiratory comorbidity 3. absence of severe daytime sleepiness and/or accidental risk that could lead to direct or indirect bodily harm * stable weight (5% variation of the weight at the time of the polysomnography done within 3 months) * patient without varicose veins, without trophic disorder that could suggest moderate to severe superficial or deep venous insufficiency (dermatitis, hypodermatitis, active or healed ulcer) * sedentary patient (patient seated more than 8 h/d Exclusion Criteria: * daily wearing of medical compression * patient with a contraindication to wearing a compression garment * patient unable to apply compression (preliminary test) * taking diuretics or venotonics * obesity (body mass index \> 30 kg/m2) * patient with leg dermatosis * patient with leg or thigh muscle trauma less than three months old * patient with sciatica, cruralgia or acute low back pain * pregnant or post-pregnancy women less than 6 months old or of childbearing age without an effective method of contraception * heart, liver or kidney failure * lymphedema of the lower limbs * cancer not considered to be in remission * history of abdominal radiotherapy

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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

  • Service des Pathologies du Sommeil Bâtiment EOLE GH Pitié-Salpêtrière

    Paris, 75013, France

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