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Application of the sensor-based Cynteract glove in the follow-up assessment of patients with chronic immune neuropathies.

Application of the sensor-based Cynteract glove in the follow-up assessment of patients with chronic immune neuropathies. - GloNeu TRIAL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00027345
Enrollment
30
Registered
2022-03-23
Start date
2022-03-11
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

G61.8

Interventions

Group 1: Patients with chronic immune neuropathies under IVIg therapy: 1st examination, under IVIg therapy at previous dose: MRC Sum Score, INCAT Overall Disability Score, Rasch-built Overall Disabil

Sponsors

Neurologische KlinikUniversitätsklinikum Aachen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) confirmed CIDP or MMN according to the latest reviewed EFNS/PNS diagnostic criteria 2) age of at least 18 years, there is no upper age limitation 3) regular therapy with IVIg at the neurological clinic of the University Hospital Aachen. 4) planned extension of the dosing interval or a planned dose reduction of IVIg therapy (clinically stable condition under established therapy regimen for =2 therapy cycles (median 4 weeks) prior to inclusion). 5) written informed consent for the storage and analysis of anonymised, patient-related clinical data

Exclusion criteria

Exclusion criteria: 1) lack of informed consent and non-fulfilment of inclusion criteria. 2) higher degree of functionally relevant systemic or hand-related previous disease/damage that would be associated with a relevant functional limitation of hand function beyond CIDP or MMN 3) other pre-existing and concomitant diseases that do not allow meaningful participation in the study (e.g. dementia)

Design outcomes

Primary

MeasureTime frame
Time (a total of at least 5 time points planned before and after therapy adjustment)

Countries

Germany

Contacts

Public ContactPascal Achenbach

Neurologische KlinikUniversitätsklinikum Aachen

pachenbach@ukaachen.de0241 800

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 5, 2026