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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04122599
Other study ID # 752/2018BO2
Secondary ID
Status Recruiting
Phase Phase 2/Phase 3
First received
Last updated
Start date July 1, 2017
Est. completion date December 31, 2019

Study information

Verified date October 2018
Source University Hospital Tuebingen
Contact Annerose Mengel, MD
Phone 004970712985354
Email annerose.mengel@med.uni-tuebingen.de
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Post stroke delirium is prevalent in 10-30% of all stroke patients. We aimed to investigate wether Melatonin 2mg may prevent post stroke delirium.


Recruitment information / eligibility

Status Recruiting
Enrollment 2000
Est. completion date December 31, 2019
Est. primary completion date November 1, 2019
Accepts healthy volunteers No
Gender All
Age group 55 Years and older
Eligibility Inclusion Criteria:

- all patients with stroke, TIA or ICH admitted to our stroke unit or intemdiate care unit

- Stroke / ICH /TIA onset <= 48h

Exclusion Criteria:

- RASS <=4

- severe dementia, psychosis or depression

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Melatonin
Melatonin for prevent post stroke delirium

Locations

Country Name City State
Germany Klinik für Neurologie Tübingen BW

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Tuebingen

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of delir prevalence 3months
Secondary Change of hospital stay 3months
Secondary Change of antipsychotic drug administration 3 months
Secondary Changed stay on stroke unit and/or intermediate care 3 months