Clinical relevance of WARP by patients whit recidive complaints after lumbar spinal fusion

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON25359

Enrollment

Registered

2014-12-01

Start date

2014-12-01

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

Recidive complaints after lumbar spinal fusion

Interventions

none

Eligibility

Inclusion criteria

Inclusion criteria: Patient whit a lumbar spinal fusion. Recidive complaints after lumbar spinal fusion. All kinds of non-ferromagnetic metal.

Exclusion criteria

Exclusion criteria: Ferromagnetic metal

Design outcomes

Primary

Measure	Time frame
Increased signal-noise ratio, contrast-noise ratio, standard deviation	—

Secondary

Measure	Time frame
Better clinical diagnostic value	—

Contacts

Public ContactDaniel Bovens

Kleine Voortstraat 3

d.bovens@atriummc.nl0648140540

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)