# Genotype/Phenotype Correlation With Focus on Lung Function in Primary Ciliary Dyskinesia (PCD)

> **NCT04717115** · — · UNKNOWN · sponsor: **University Hospital Muenster** · enrollment: 1500 (estimated)

## Conditions studied

- Ciliary Motility Disorders
- Primary Ciliary Dyskinesia

## Interventions

- **GENETIC:** Genetic diagnosis

## Key facts

- **NCT ID:** NCT04717115
- **Lead sponsor:** University Hospital Muenster
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2019-11-01
- **Primary completion:** 2023-06-30
- **Final completion:** 2023-11-30
- **Target enrollment:** 1500 (ESTIMATED)
- **Last updated:** 2022-07-05

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## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04717115

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04717115, "Genotype/Phenotype Correlation With Focus on Lung Function in Primary Ciliary Dyskinesia (PCD)". Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/clinical/NCT04717115. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*