# Genetic Analysis of Oculocerebrorenal Syndrome of Lowe

> **NCT00359515** · — · COMPLETED · sponsor: **National Human Genome Research Institute (NHGRI)** · enrollment: 120 (—)

## Conditions studied

- Lowe Syndrome

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT00359515
- **Lead sponsor:** National Human Genome Research Institute (NHGRI)
- **Sponsor class:** NIH
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2001-02-17
- **Primary completion:** —
- **Final completion:** 2009-02-03
- **Target enrollment:** 120 (—)
- **Last updated:** 2017-07-02


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00359515

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00359515, "Genetic Analysis of Oculocerebrorenal Syndrome of Lowe". Retrieved via AI Analytics 2026-06-09 from https://api.ai-analytics.org/clinical/NCT00359515. Licensed CC0.

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