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Correlation between congenital cytomegalovirus infection and mutation of GJB2 gene

Correlation between congenital cytomegalovirus infection and mutation of GJB2 gene

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OCC-09000489
Enrollment
Unknown
Registered
2009-08-13
Start date
2008-12-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital cytomegalovirus infection

Interventions

study group:To gather and test the blood and urine samples of neonates
control group:To gather and test the blood and urine samples of neonates

Sponsors

The Chongqing Medical University, Chongqing, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 14 Years

Inclusion criteria

Inclusion criteria: The neonates less than 14 days age with cytomegalovirus infection.

Exclusion criteria

Exclusion criteria: Neonates with hypoxic ischemic encephalopathy, purulent meningitis, bilirubin encephalopathy, apparent abnormality of external auditory canal, III or IV IVH or Combination with other virus infection except for cytomegalovirus infection.

Design outcomes

Primary

MeasureTime frame
The mutation rate of GJB2 gene;brainstem auditory evoked potential;real-time Polymerase Chain Reaction;TORCH detection;

Countries

China

Contacts

Public ContactLuquan Li
liluquan456@yahoo.com.cn+86 13678433408

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026