# Prognostic Significance of Mutation Type and Chromosome Fragility in Fanconi Anemia

> **NCT06490510** · — · COMPLETED · sponsor: **Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau** · enrollment: 227 (actual)

## Conditions studied

- Fanconi Anemia

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT06490510
- **Lead sponsor:** Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2024-05-16
- **Primary completion:** 2024-06-18
- **Final completion:** 2024-06-18
- **Target enrollment:** 227 (ACTUAL)
- **Last updated:** 2024-07-08


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06490510

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06490510, "Prognostic Significance of Mutation Type and Chromosome Fragility in Fanconi Anemia". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT06490510. Licensed CC0.

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