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NCT04966858: i-STRONG

Individualized Study of Refeeding to Optimize iNpatient Gains

ENROLLING BY INVITATION NA Last updated 23 January 2026
What this trial tests

NA trial testing Individualized Caloric Refeeding (ICR) in Atypical Anorexia Nervosa in 74 participants. Enrolling by invitation.

Timeline
12 October 2021
Primary endpoint
3 June 2025
31 March 2026

Quick facts

Lead sponsorUniversity of California, San Francisco
PhaseNA
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment74
Start date12 October 2021
Primary completion3 June 2025
Estimated completion31 March 2026
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of California, San Francisco

Who can join

Adults 12 to 24, any sex, with Atypical Anorexia Nervosa. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Atypical Anorexia Nervosa

Currently open trials in the same condition.

Other University of California, San Francisco trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04966858.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing