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NCT05873309Completed

The Role of OXytocin in Acute Ischemic Stroke reconvAlesceNcE: The ROXANE Study

Source: ClinicalTrials.gov · Last updated 4 Mar 2025

Brief summary (registry, in English)

Evidence suggests that oxytocin has a neuroprotective role on a systemic and cellular level in the context of acute ischemic stroke (AIS). The investigators therefore hypothesize that high levels of circulating oxytocin measured within the first 72 hours after symptom onset are associated with lower mortality and favorable outcome in acute ischemic stroke.

Status (registry)
Completed
Study type
Observational
Enrollment
386 (actual)
First submitted
15 May 2023
Start date
26 Apr 2023
Primary completion date
23 Sept 2024
Lead sponsor
University Hospital, Basel, Switzerland
Diseases
Stroke
NCT number
NCT05873309

What you commit to

  • Study type: Observational
  • Participants enrolled: 386
  • From 26 Apr 2023 to the primary completion date, 23 Sept 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Hemorrhagic stroke or patients discharged from the hospital with a diagnosis different from ischemic stroke (i.e., stroke mimics)

Other

  • Patients below 18 years
  • Missing informed consent

Who the study is looking for

  • Rapid onset of a focal neurologic deficit, with signs or symptoms persisting beyond 24 hours and not associated with infection, trauma, or tumor of the brain, severe metabolic disorders, or chronic degenerative neurologic disease; or
  • the development of an acute focal neurologic deficit persisting \>24 hours in conjunction with brain imaging consistent with acute ischemic stroke. The CT or MRI may either show a new infarct or no change from the study performed at entry, i.e., the diagnosis is clinical and does not require CT/MRI confirmation. Secondary hemorrhagic infarction is permissible.
  • First blood sample at the stroke unit is taken within 24 hours from symptom onset.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital Basel
Coordinator of this site? Confirm its status
BaselSwitzerlandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.