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WGS of Korean Idiopathic Bronchiectasis

NCT03809091 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2019-01-25

No results posted yet for this study

Summary

Whole genome sequencing of Korean patients with idiopathic bronchiectasis and their family will perform to identify disease-causing variants.

Conditions

Interventions

DIAGNOSTIC_TEST

Whole genome sequencing

Whole genome sequencing of patients and their family will be performed. Among the variants detected by WGS, disease-causing variants will be analyzed by using segregation analysis.

Sponsors & Collaborators

  • Seoul National University Hospital

    lead OTHER

Principal Investigators

  • Jae-June Yim, MD · Division of Pulmonology and Critical Care Medicine, Seoul National University College of Medicine

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-31
Primary Completion
2021-08-31
Completion
2021-12-31

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03809091 on ClinicalTrials.gov