# Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease

> **NCT04620980** · — · UNKNOWN · sponsor: **Neuromed IRCCS** · enrollment: 600 (estimated)

## Conditions studied

- Parkinson Disease

## Interventions

- **DIAGNOSTIC_TEST:** targeted resequencing

## Key facts

- **NCT ID:** NCT04620980
- **Lead sponsor:** Neuromed IRCCS
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2021-06-15
- **Primary completion:** 2023-09-30
- **Final completion:** 2024-05-17
- **Target enrollment:** 600 (ESTIMATED)
- **Last updated:** 2022-09-28


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04620980

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04620980, "Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT04620980. Licensed CC0.

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