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NCT06183567Completed

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

Source: ClinicalTrials.gov · Last updated 8 Oct 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
62 (actual)
First submitted
13 Dec 2023
Start date
30 Nov 2023
Primary completion date
30 Dec 2025
Lead sponsor
Umraniye Education and Research Hospital
Diseases
Stroke
NCT number
NCT06183567

What you commit to

  • Study type: Interventional
  • Participants enrolled: 62
  • From 30 Nov 2023 to the primary completion date, 30 Dec 2025
  • 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.

Prior treatment

  • Previous known history of severe neurological disease
  • Previously known carotid artery stenosis

Other illness

  • Chronic renal failure
  • Presence of intracranial hemorrhage
  • Presence of bleeding diathesis
  • Failure to clearly show the site of vascular occlusion on diagnostic imaging results
  • 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

Other

  • EF less than 40
  • Pre-procedure GCS ≤ 8 and intubated patients
  • 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
  • Pregnant patients
  • Patients without consent

Who the study is looking for

  • Presence of cerebral ischemic embolism within the first 6 hours
  • ASA 1-4
  • Body mass index below 30 kg m-2
  • NIHSS score ≥ 10
  • Presence of isolated/combined occlusion at any level of the anterior circulation internal carotid or middle cerebral artery

Age in the registry: 18 years to 80 years · 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
Umraniye Education and Research Hospital
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

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