# Genetic Disease Gene Identification

> **NCT00916903** · — · TERMINATED · sponsor: **State University of New York - Upstate Medical University** · enrollment: 176 (actual)

## Conditions studied

- Congenital Vertical Talus
- Familial Encephalopathy With Neuroserpin Inclusion Bodies
- Idiopathic Generalised Epilepsy
- Familial Dementia
- X-linked Mental Retardation

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT00916903
- **Lead sponsor:** State University of New York - Upstate Medical University
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** TERMINATED
- **Start date:** 2005-10
- **Primary completion:** 2015-04
- **Final completion:** 2015-07
- **Target enrollment:** 176 (ACTUAL)
- **Why stopped:** Lack of funding.
- **Last updated:** 2024-01-02


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00916903

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00916903, "Genetic Disease Gene Identification". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT00916903. Licensed CC0.

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