# Identification of a New Gene Involved in Hereditary Lipodystrophy

> **NCT02056912** · NA · COMPLETED · sponsor: **University Hospital, Bordeaux** · enrollment: 2 (actual)

## Conditions studied

- Lipodystrophy

## Interventions

- **GENETIC:** Amplification by PCR and direct sequencing on the entire coding sequence and intron-exons boundaries of the candidate gene
- **BIOLOGICAL:** Perform blood cells and fibroblasts biochemical and immuno-labeled investigations

## Key facts

- **NCT ID:** NCT02056912
- **Lead sponsor:** University Hospital, Bordeaux
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2014-01
- **Primary completion:** 2014-01
- **Final completion:** 2014-01
- **Target enrollment:** 2 (ACTUAL)
- **Last updated:** 2015-01-14


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02056912

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02056912, "Identification of a New Gene Involved in Hereditary Lipodystrophy". Retrieved via AI Analytics 2026-06-09 from https://api.ai-analytics.org/clinical/NCT02056912. Licensed CC0.

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