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Clinical Trials in Turkey / NCT06183567
Active, not recruiting Not applicable

The Effect of Sedoanalgesia and General Anaesthesia on Early Neurological Recovery in Acute Ischaemic Stroke Patients Undergoing Endovascular Thrombectomy

NCT06183567 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2023-11-30
Last updated
2025-11-19

Condition(s) studied

Ischemic StrokeAnesthesiaNeurologic Symptoms

Investigational drug(s) / intervention(s)

Sedoanalgesiageneral anesthesia

Sedoanalgesia: In Acute Ischemic Stroke Patients Undergoing Endovascular Thrombectomy, the procedure was performed under sedoanalgesia. The procedure was continued with mean arterial pressure, heart rate, pulse oximetry and BIS monitoring.

general anesthesia: In Acute Ischemic Stroke Patients Undergoing Endovascular Thrombectomy, the procedure was performed under general anesthesia. The procedure was continued with mean arterial pressure, heart rate, pulse oximetry and BIS monitoring.

Study summary

The hypothesis of this study is that sedoanalgesia will provide better early neurological recovery than general anaesthesia in acute ischaemic stroke patients undergoing endovascular thrombectomy and to investigate the haemodynamic data of both anaesthetic methods.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: 1. Presence of cerebral ischemic embolism within the first 6 hours 2. ASA 1-4 3. Body mass index below 30 kg m-2 4. NIHSS score ≥ 10 5. Presence of isolated/combined occlusion at any level of the anterior circulation internal carotid or middle cerebral artery Exclusion Criteria: * Chronic renal failure * EF less than 40 * Presence of intracranial hemorrhage * Previous known history of severe neurological disease * Presence of bleeding diathesis * Pre-procedure GCS ≤ 8 and intubated patients * Failure to clearly show the site of vascular occlusion on diagnostic imaging results * Clinical or imaging evidence of vascular occlusion that is not internal carotid artery or middle cerebral artery * Absence of gag reflex, loss of airway protective reflex, inadequate saliva swallowing * History of lung infection, advanced COPD or respiratory failure * Known history of aspiration due to vomiting, * Known history of difficult airway * In the presence of known intolerance or allergy to certain drugs for sedation, analgesia or both * Previously known carotid artery stenosis * Pregnant patients * Patients without consent

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Umraniye Education and Research Hospital Istanbul Umraniye

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06183567 on ClinicalTrials.gov ↗ ← All trials in Turkey