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New equation could simplify salt monitoring for kidney dialysis patients

NCT ID NCT05955417

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 aims to create and test a new mathematical formula that estimates how much sodium (salt) people on peritoneal dialysis consume. The researchers will enroll 30 adults who have been on peritoneal dialysis for at least three months and have no remaining kidney function. If the equation proves accurate, it could offer a simpler way to monitor dietary sodium without relying on patient recall or food diaries.

What this could mean

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

What this could lead to
If successful, this equation could help doctors better manage sodium intake in peritoneal dialysis patients without needing detailed diet records.
What could go wrong
This is a small, early-stage study with only 30 participants, so the equation may not be accurate for all patients or in different settings.

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.

Participants

30 people

The number who actually took part.

Started

Aug 2023

Finished

Jan 2025

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.

Who is studied

Peritoneal Dialysis Patients

Ages

18 to 80 years

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: * Peritoneal dialysis vintage \>3 months. * 18-80 years old. * No residual renal function (urine volume\<200ml/day). Exclusion Criteria: * Peritonitis in the past month. * Acute systemic infection, cardio-cerebrovascular complications and surgical trauma in the past month. * Uncorrected hyponatremia (blood sodium\<130mmol/L). * Prescribed with sodium bicarbonate. * Prescribed with glucocorticoids and aldosterone antagonists. * Dysfunction of peritoneal dialysis catheter. * Malignant tumor receiving radiotherapy and chemotherapy, severe dyspepsia or eating disorder. * Body fluid loss due to vomit, diarrhea, massive sweating, or other causes. * Cannot follow the research scheme. * Refuse to participate in this study.

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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

  • Peking University First Hospital

    Beijing, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.