Skip to content

Specturi Device - Feasibility study

Specturi Device - Feasibility study - Specturi feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON54632
Enrollment
10
Registered
2015-11-16
Start date
2020-01-27
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

English disease

Interventions

&nbsp
Specturi urine collection device&nbsp

Sponsors

Capturin Distributie B.V.
Lead Sponsor

Eligibility

Age
No minimum to 1 Years

Inclusion criteria

Inclusion criteria:  Neonates admitted to the neonatology unit of the Maternity care department of  Rijnstate Hospital and Radboud Hospital Nijmegen Medical indication for urine testing using a urine collection device Informed consent from parents 

Exclusion criteria

Exclusion criteria:  No informed consent Defective skin in genital region Three previous test in the same subject 

Design outcomes

Primary

MeasureTime frame
Clinical feasibility of the urine collection device, indicated by staff and parents

Secondary

MeasureTime frame
Skin reactions and skin irritability

Countries

Netherlands

Contacts

Public Contact- Pediatric Research Unit Radboudumc

Radboud Universitair Medisch Centrum

pediatricresearchunit@radboudumc.nl024-3655700

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)