N-Care Project: Enhancing Asian-Pacific Collaboration

Recruiting

• Conditions: Whole Genome Sequencing; Genetic Disease; Critical Care, Intensive Care; Nanopore Sequencing

• Registration Number: NCT06821386
• Lead Sponsor: National Taiwan University Hospital

Brief Summary

Through Asian-Pacific multinational collaboration, we aim to utilize third-generation genome sequencing to rapidly diagnose genetic diseases in critically ill infants and young children, achieving the goal of early diagnosis for targeted treatment.

Detailed Description

A group of individuals with specific characteristics was selected. Genetic studies were arranged for participants who provided their consent.

Study Timeline

• Status Verified: 2025-02
• Study First Submitted: 2025-02-03
• Study First Submitted QC: 2025-02-09
• Study First Posted: 2025-02-12
• Study Start: 2025-02-17
• Last Update Submitted: 2025-02-18
• Last Update Posted: 2025-02-20
• Primary Completion: 2025-12-31
• Study Completion: 2032-12-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

1. Age: infant/newborn less than 18 months

2. Admitted to intensive care unit

3. At least one of the following conditions A. Specific anomaly highly suggestive of a genetic etiology

   • Multiple birth defects
   • Single major malformation that required intervention (surgery or medication)
   • Significantly abnormal EKG
   • Significant hypotonia

B. Children with high-risk stratification on assessment of a Brief Resolved Unexplained Event (BRUE) with any of the following:

• Recurrent severe infection events
• Recurrent or prolonged seizures
• Unexplained cardiopulmonary resuscitation (CPR)
• Suspect inborn error of metabolism

Exclusion Criteria

1. Infants with a definitive non-genetic diagnosis: ex as below A. An infection with normal response to therapy B. Isolated prematurity C. Transient hypoglycemia D. Isolated unconjugated hyperbilirubinemia E. Isolated Transient Neonatal Tachypnea F. Those where the clinical course can be explained without genetic testing
2. Confirmed genetic diagnosis explains illness
3. Lack of consent: Families who do not consent to genetic testing or data sharing.
4. Infants without sufficient DNA sample quality/quantity: Where the quality or quantity of the DNA sample is inadequate for sequencing.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Positive yield rate	9 days after enrollment	The percentage of individuals who test positive among the long-read sequencing exam

Trial Locations

Locations (1)

National Taiwan University Hospital; 🇨🇳 Taipei, Taiwan