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Effect of Postoperative Prolonged Sedation With Dexmedetomidine After Successful Reperfusion With Endovascular Thrombectomy on Long-term Prognosis in Patients With Acute Ischemic Stroke (PPDET)

Who is this study for? Adult patients with Acute Ischemic Stroke
What treatments are being studied? Dexmedetomidine
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

Dexmedetomidine can attenuate the activity of the sympathetic nervous system under stress response and improve ischemia-reperfusion injury. The investigators hypothesized that the prolonged sedation of dexmedetomidine after successful reperfusion of endovascular thrombectomy may improve the clinical outcome of acute ischemic stroke patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• 2≤NIHSS≤25

• mRS score before stroke was less than 3

• Acute ischemic stroke (including anterior circulation)

• mTICI rate 2b or 3

• According to the 2018 AHA/ASA guidelines for the management of acute ischemic stroke, patients who plan to receive mechanical thrombectomy under local anesthesia and sedation

• Informed consent was signed by patient or legal representative

Locations
Other Locations
China
Beijing ChaoYang Hospital
RECRUITING
Beijing
Contact Information
Primary
Lina Yang
Thoth_safin@sina.com
18611635556
Time Frame
Start Date: 2024-03-01
Estimated Completion Date: 2026-12
Participants
Target number of participants: 368
Treatments
Experimental: Intervention group
Dexmedetomidine 0.1\~1.0 μg/kg/h for 24h after patients finished endovascular thrombectomy and returned to ICU. Maintain Ramsay score 2-3.
Placebo_comparator: Control group
An equal dose of saline 24h after patients finished endovascular thrombectomy and returned to ICU. If the Ramsay sedation score is 1, propofol will be administrated to maintain the Ramsay sedation score at 2 to 3.
Related Therapeutic Areas
Sponsors
Leads: Beijing Chao Yang Hospital

This content was sourced from clinicaltrials.gov