# Metabolic Consequences of Heterozygous Hereditary Fructose Intolerance

> **NCT02979106** · NA · COMPLETED · sponsor: **University of Lausanne** · enrollment: 18 (actual)

## Conditions studied

- Hereditary Fructose Intolerance
- Fructose Metabolism, Inborn Errors
- Glucose Metabolism Disorders

## Interventions

- **OTHER:** Test meal

## Key facts

- **NCT ID:** NCT02979106
- **Lead sponsor:** University of Lausanne
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2015-01
- **Primary completion:** 2016-01
- **Final completion:** 2016-11
- **Target enrollment:** 18 (ACTUAL)
- **Last updated:** 2019-07-17


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02979106

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02979106, "Metabolic Consequences of Heterozygous Hereditary Fructose Intolerance". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT02979106. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
