# A P2X7R Single Nucleotide Mutation Promotes Chronic Allograft Vasculopathy

> **NCT02082821** · — · COMPLETED · sponsor: **Boston Children's Hospital** · enrollment: 200 (actual)

## Conditions studied

- Cardiac Allograft Vasculopathy

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT02082821
- **Lead sponsor:** Boston Children's Hospital
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2014-01
- **Primary completion:** 2019-08
- **Final completion:** 2020-12
- **Target enrollment:** 200 (ACTUAL)
- **Last updated:** 2021-03-03


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02082821

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02082821, "A P2X7R Single Nucleotide Mutation Promotes Chronic Allograft Vasculopathy". Retrieved via AI Analytics 2026-06-05 from https://api.ai-analytics.org/clinical/NCT02082821. Licensed CC0.

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