# Genetic Risk Factors of the Sneddon Syndrome

> **NCT06850519** · — · COMPLETED · sponsor: **Karl Landsteiner University of Health Sciences** · enrollment: 40 (actual)

## Conditions studied

- Sneddon Syndrome

## Interventions

- **GENETIC:** Exome Sequencing and Sanger Sequencing

## Key facts

- **NCT ID:** NCT06850519
- **Lead sponsor:** Karl Landsteiner University of Health Sciences
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2021-05-12
- **Primary completion:** 2024-11-08
- **Final completion:** 2024-11-08
- **Target enrollment:** 40 (ACTUAL)
- **Last updated:** 2025-02-27

## Collaborators

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## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06850519

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06850519, "Genetic Risk Factors of the Sneddon Syndrome". Retrieved via AI Analytics 2026-07-16 from https://api.ai-analytics.org/clinical/NCT06850519. Licensed CC0.

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