# The Study of the Phenotype of Hereditary Xerocytosis

> **NCT06892171** · NA · RECRUITING · sponsor: **Centre Hospitalier Universitaire, Amiens** · enrollment: 20 (estimated)

## Conditions studied

- Xerocytosis
- Phenotype
- Genotype

## Interventions

- **BIOLOGICAL:** Blood sample

## Key facts

- **NCT ID:** NCT06892171
- **Lead sponsor:** Centre Hospitalier Universitaire, Amiens
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2025-03-01
- **Primary completion:** 2028-03
- **Final completion:** 2028-03
- **Target enrollment:** 20 (ESTIMATED)
- **Last updated:** 2025-04-30

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06892171

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06892171, "The Study of the Phenotype of Hereditary Xerocytosis". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT06892171. Licensed CC0.

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