# Mutation p.Ile112Thr : Discrepancy Between Factor IX Level and Bleeding Phenotype

> **NCT03946384** · — · UNKNOWN · sponsor: **Centre Hospitalier Universitaire Dijon** · enrollment: 12 (estimated)

## Conditions studied

- Hemophilia B

## Interventions

- **OTHER:** data collection

## Key facts

- **NCT ID:** NCT03946384
- **Lead sponsor:** Centre Hospitalier Universitaire Dijon
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2019-06
- **Primary completion:** 2019-10
- **Final completion:** 2019-10
- **Target enrollment:** 12 (ESTIMATED)
- **Last updated:** 2019-05-10


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03946384

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03946384, "Mutation p.Ile112Thr : Discrepancy Between Factor IX Level and Bleeding Phenotype". Retrieved via AI Analytics 2026-07-07 from https://api.ai-analytics.org/clinical/NCT03946384. Licensed CC0.

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