# Neonatal Screening of Biotinidase Deficiency: Genotype-phenotype Correlation and Clinical Follow-up

> **NCT06723925** · — · RECRUITING · sponsor: **IRCCS Azienda Ospedaliero-Universitaria di Bologna** · enrollment: 180 (estimated)

## Conditions studied

- Biotinidase Deficiency

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT06723925
- **Lead sponsor:** IRCCS Azienda Ospedaliero-Universitaria di Bologna
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2021-04-21
- **Primary completion:** 2026-10-31
- **Final completion:** 2026-12-31
- **Target enrollment:** 180 (ESTIMATED)
- **Last updated:** 2026-03-12


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06723925

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06723925, "Neonatal Screening of Biotinidase Deficiency: Genotype-phenotype Correlation and Clinical Follow-up". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT06723925. Licensed CC0.

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