A Study on the Preventive Effect of Electroacupuncture Combined With Dexmedetomidine in Post-stroke Depression

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorMin Su

About this trial

Post-stroke depression (PSD) is a common neuropsychiatric complication following stroke and has emerged as a major public health concern due to its adverse impact on post-stroke prognosis. Clinical studies have confirmed that early intervention with electroacupuncture can significantly reduce PSD incidence and alleviate depressive severity. Mechanistically, electroacupuncture exerts antidepressant effects through inhibition of the endoplasmic reticulum stress pathway and attenuation of neuronal apoptosis. Dexmedetomidine, a highly selective α₂-adrenergic receptor agonist, not only provides sedation and analgesia but also confers neuroprotective actions, including anti-inflammatory, anti-apoptotic, and blood-brain barrier protective effects. Its efficacy in preventing postpartum depression has been clinically validated. Given the substantial burden of PSD and the limitations of existing preventive approaches, the present study aims to investigate the value of a combined electroacupuncture and dexmedetomidine strategy for PSD prevention, with the goal of developing a safe and effective integrative treatment regimen for this frequent post-stroke complication.

Eligibility criteria

Qualifiers

Ischemic stroke with a disease course of less than 2 weeks;

Patients with high-risk PSD;

The patient can accept the treatment plan described in this trial and sign the informed consent form.

Disqualifiers

Cognitive impairment;

Severe aphasia or significant language impairment;

Disturbance of consciousness;

History of psychiatric disorders, including but not limited to depression, schizophrenia, and bipolar disorder;

Trial design

Treatments tested in this trial

  • Dexmedetomidine
  • Electropuncture
  • Normal Saline (NS)
  • Shame electropuncture

Treatment groups

231 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Min Su

Lead sponsor

First Affiliated Hospital of Chongqing Medical University

Sponsor institution