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New study tests safer refeeding for teens with atypical anorexia

NCT ID NCT04966858

Disease control Sponsor: University of California, San Francisco Source: ClinicalTrials.gov ↗

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study compares two ways of reintroducing food (refeeding) to hospitalized patients aged 12-24 with atypical anorexia nervosa. The goal is to see which method helps patients reach medical stability faster and with fewer side effects. Participants will be followed for one year to track recovery.

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 74 people

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

Started

Oct 2021

Expected to finish

Mar 2026

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

12 to 24 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: * Age 12-24 yrs * Meets Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria for AAN * Hospitalized with medical instability, as defined by: 1. night time heart rate (HR) \<45 bpm, 2. systolic blood pressure (SBP) \<90 mmHg, 3. temperature \<35.6° C, 4. orthostatic Δ HR \>35 bpm, or 5. orthostatic Δ SBP \>20 mmHg Exclusion Criteria: * Bulimia nervosa * Current pregnancy * Chronic disease (e.g. immune, renal disease) * Acute/active suicidality or psychosis * Hospital admissions for refeeding in the prior 6 mo.

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Conditions

The condition(s) this trial relates to.

anorexia nervosa Malnutrition

As listed by the trial registrant

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

Atypical anorexia nervosa

How to take part

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

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Stanford University Lucille Packard Children's Hospital

    Palo Alto, California, 94304, United States

  • University of California, San Francisco Benioff Children's Hospital

    San Francisco, California, 94158, United States

More trials for these conditions

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