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Prognostic Markers of Post-Stroke Depression (PROMoSD)

R

Ruhr University of Bochum

Status

Enrolling

Conditions

Acute Ischemic Stroke

Treatments

Diagnostic Test: Transcranial sonography.

Study type

Observational

Funder types

Other

Identifiers

NCT05580198
20-6862

Details and patient eligibility

About

Single-center prospective observational study investigating the association of brainstem raphe hypoechogenicity detected by transcranial sonography and post-stroke depression three months after an acute ischemic stroke.

Full description

Post-stroke depression (PSD) is an important complication after a stroke. Despite significant limitations between studies of PSD risk factors, stroke severity or post-stroke disability, prior depressive episodes, and female sex are arguably the most well-known risk factors for developing PSD, although the predictive value of these factors is limited.

A hypoechogenic brainstem raphe (BR) detected by transcranial sonography (TCS) is associated with depressive symptoms in distinct diseases but is also common with approximately 25% of the non-depressed population in Europe. The primary aim of this study is to investigate the association between BR hypoechogenicity and PSD occurrence in a prospective observational study design.

Enrollment

105 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Acute ischemic stroke with the onset of symptoms within the past 14 days
  • Diagnosis of AIS is confirmed by brain imaging, either computer tomography or magnetic resonance imaging

Exclusion criteria

  • Insufficient transtemporal bone window for transcranial sonography examination

Trial design

105 participants in 2 patient groups

BRH+
Description:
Acute ischemic stroke patients with brainstem raphe hypoechogenicity.
Treatment:
Diagnostic Test: Transcranial sonography.
BRH-
Description:
Acute ischemic stroke patients without brainstem raphe hypoechogenicity.
Treatment:
Diagnostic Test: Transcranial sonography.

Trial contacts and locations

1

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Central trial contact

Daniel Richter, Dr,

Data sourced from clinicaltrials.gov

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