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Genetic characteristics of Primary Ciliary Dyskinesia.

Sequencing study in Primary Ciliary Dyskinesia.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON24319
Enrollment
83
Registered
2011-11-11
Start date
2012-01-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Primary Ciliary Dyskinesia

Interventions

None listed

Sponsors

VU University Medical Center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Primary Ciliary Dyskinesia.

Exclusion criteria

Exclusion criteria: Other recessive hereditary disorders.

Design outcomes

Primary

MeasureTime frame
1. Accuracy of MPS in detecting PCD mutation (validation); 2. Possible pathogenic mutations causing PCD.

Contacts

Public ContactT. Paff

Postbus 7057

t.paff@vumc.nl+31 (0)20 4445491

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)