By InvitationNot Applicable

Individualized Study of Refeeding to Optimize iNpatient Gains

United States74 participantsStarted 2021-10-12

Plain-language summary

The primary purpose of the trial is to compare the efficacy and safety of Individualized Caloric Refeeding (ICR) to the new standard of care, Higher Calorie Refeeding (HCR), in hospitalized patients with atypical anorexia nervosa (AAN), and clinical remission over one year of follow-up.

Who can participate

Age range12 Years – 24 Years

SexALL

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Inclusion criteria

✓. night time heart rate (HR) \<45 bpm,
✓. systolic blood pressure (SBP) \<90 mmHg,
✓. temperature \<35.6° C,
✓. orthostatic Δ HR \>35 bpm, or
✓. orthostatic Δ SBP \>20 mmHg

What they're measuring

Time to Achieve Medical Stability in Hospital

Timeframe: Inpatient hospitalization from day of admission to day of discharge, average 1-2 weeks

Trial details

NCT IDNCT04966858

SponsorUniversity of California, San Francisco

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-06-03

View on ClinicalTrials.gov More Atypical Anorexia Nervosa trials