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Predicting corticosteroid response in inflammatory neuropathies

Predicting corticosteroid response in inflammatory neuropathies - PRECRIN

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON33384
Enrollment
6
Registered
2009-09-16
Start date
2009-05-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

inflammatory demyelinating neuropathy neuropathy

Interventions

All patients and controls recieve 40 mg dexamethasone daily during 4 days

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Adult patients >

Exclusion criteria

Exclusion criteria: - Other diseases known to cause neuropathy - Use of drugs which are known to cause neuropathy - Neurophysiological evidence of carpal tunnel syndrome - Use of immunomodulatory drugs in the last 6 months or IVIg in the last 2 months. - Refusal to give informed consent or withdrawal of previously given permission - Legally incompetent adult

Design outcomes

Primary

MeasureTime frame
1. Change in excitability indicating hyperpolarization 2. Change in severity and number of conduction blocks

Secondary

MeasureTime frame
1. Conduction velocity 2. MRC sum score (muscle strength) 3. INCAT sensory sum score (sensory deficit score) 4. ALDS (Amsterdam Linear Disability Scale) 5. INCAT disability scale (a frequently used disability scale in inflammatory neuroapathies) 6. any adverse event or reaction

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)