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DELirium, Incidence, preVEntion and pRogression During Acute Intensive Neurological -Neurosurgical Rehabilitation

DELirium, Incidence, preVEntion and pRogression During Acute Intensive Neurological -Neurosurgical Rehabilitation (Delirinzidenz Und Verlauf während Des Aufenthaltes in Der Neurologisch- Neurochirurgischen Frührehablilitation Der Phase B (NNFR))

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07070310
Acronym
DeliVeriNN
Enrollment
210
Registered
2025-07-17
Start date
2025-08-15
Completion date
2029-02-15
Last updated
2025-07-22

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

Conditions

Neurological Conditions

Brief summary

In this longitudinal cohort study the incidence of delirium is assessed for all patients being admitted to the acute intensive neurological-neurosurgical rehabilitation over 3 years. Delirium assessment will be performed daily from admission to discharge. Patients will be divided into 3 groups, according to the presentation of delirium on admission, during the course or not any during the stay in acute rehabilitation and compared regarding the treatment and outcome.

Interventions

None listed

Sponsors

Heart Centre Rotenburg
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Any patient admitted to acute neurological-seurosurgical rehabilitation

Exclusion criteria

* : patients with level of consciousness of coma or vegetative state

Design outcomes

Primary

MeasureTime frame
incidence of delirium3 years

Countries

Germany

Contacts

Primary ContactCaroline Renner, Priv.-Doz. Dr. med
c.renner@hkz-rotenburg.de+49-6623-88-0

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026