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Can acupressure calm restless legs and itching in dialysis?

NCT ID NCT07814443

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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 11, 2026 · Last updated Sep 11, 2026

Summary

Researchers test whether combined traditional and paraspinal acupressure can reduce restless legs syndrome and itching in people undergoing hemodialysis. Seventy adults with at least moderate symptoms join the randomized trial. Half receive the acupressure intervention plus routine dialysis care, and half receive routine care alone. The team measures changes in symptom severity using standard rating scales.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
vibration-assisted acupressure on traditional and paraspinal acupoints
What this could lead to
If it works, acupressure could offer a drug-free way to ease restless legs and itching for people on hemodialysis.
What could go wrong
This is a small, single-center study of 70 people. Acupressure may not outperform routine care, and results may not apply to other dialysis patients.

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

About 70 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Apr 2027

An estimate. End dates often move.

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

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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 1. Patients more than 18 years old on hemodialysis treatment for more than 2 sessions per week. 2. The patients on hemodialysis for more than 3 months 3. The patients who complain of restless leg syndrome and pruritus. 4. RLS diagnosis meeting the diagnostic criteria defined by the International Restless Legs Syndrome Study Group (IRLSSG). 5. At least moderate RLS symptoms (IRLS - total score ≥ 11) 6. Patients who score more than five on the 5D Pruritus scale. 7. Patient with a history of pruritus for more than 3 months. Exclusion Criteria 1. Patients with impaired skin integrity. 2. Patients with skin lesions in areas involved in acupressure therapy. 3. Patients with neurological deficits as perception of pain, may differ from other patients. 4. Patients with a body mass index (BMI) of more than \> 30 kg/m². 5. Patients with malignancy. 6. Patients with Jaundice.

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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.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

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  3. A doctor treating you

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Contacts and locations

Locations

  • Al-Hussien Hemodialysis center

    Dhi-Qar, Dhi Qar, 64001, Iraq

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