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OptiNIV - Retrospective investigation of post-hospital intensive care in neurological patients

OptiNIV - Retrospective investigation of post-hospital intensive care in neurological patients - OptiNIV

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00030580
Enrollment
250
Registered
2022-10-28
Start date
2022-01-09
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

Previous inpatient treatment in early neurological rehabilitation with neurological rehabilitation diagnosis and presence of mechanical ventilation and/or tracheal cannula at discharge from neurological early rehabilitation

Interventions

Group 1: The different primary and secondary endpoints are collected on the one hand in a telephone interview [current status] and on the other hand taken from the medical record of the discharging cl

Sponsors

Klinikum der Universität München, Campus Großhadern
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age of majority, previous inpatient treatment in the neurological early rehabilitation of one of the partner hospitals with neurological rehabilitation diagnosis and presence of mechanical ventilation and/or tracheal cannula at the time of discharge from the clinic, discharge to out-of-hospital intensive care in the period 01.01.2019 - 30.06.2021

Exclusion criteria

Exclusion criteria: Palliative treatment/life expectancy according to medical assessment < 12 months at the time of discharge, weaning/decanulation medically ruled out (e.g. high cervical paraplegia, laryngeal tumour), pre-existing out-of-hospital intensive care prior to inpatient stay in one of the partner hospitals, progressive neuromuscular disease (e.g. muscular dystrophy, ALS).

Design outcomes

Primary

MeasureTime frame
Rate of patients who could be weaned off mechanical ventilation and/or tracheal cannula 6 months (and one year) after the start of treatment in out-of-hospital intensive care (and time of weaning after discharge from neurological early rehabilitation).

Secondary

MeasureTime frame
Secondary outcome measures (each collected by means of checklists or standardised scores, partly also at the time of discharge [according to file/medical record; marked with "(E)"], all at the time of the survey [telephone interview]): - TC and ventilator status and modalities (E). - Extent of care Accesses (e.g. PEG) (E) - mortality - Neurological status (GOS-E) (E) - Activities of daily living (ATL) (E) - Quality of life (QOL) - Relative burden - Care situation (use of AIP / living arrangements) - Satisfaction with the care situation - Complications/side effects - Information on health insurance (E)

Countries

Germany

Contacts

Public ContactAndreas Bender

Neurologische KlinikKlinikum der Universität München

anbender@med.uni-muenchen.de089440074833

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026