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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02677415
Other study ID # QML20150508
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 2016
Est. completion date December 2022

Study information

Verified date September 2021
Source Beijing Tiantan Hospital
Contact Ruquan Han, M.D., Ph.D.
Phone 8610-67096660
Email ruquan.han@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Recent observational studies have found an association between general anaesthesia and increased post-operative mortality in acute ischemic stroke patients undergoing endovascular treatment. It is unknown whether there is a causal relationship in this observation. The investigators are performing a large randomised trial of general versus local anaesthesia to definitively answer the question of whether anaesthetic type alters perioperative outcome.


Recruitment information / eligibility

Status Recruiting
Enrollment 640
Est. completion date December 2022
Est. primary completion date December 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with AIS scheduled to receive emergency endovascular treatment, older than 18; the onset time is within 12 hours. Exclusion Criteria: - Radiological ambiguity concerning infarction and vessel occlusion. - Additional intracerebral hemorrhage. - Posterior circulation infraction. - Coma on admission (Glasgow coma score less than 8). - NIHSS less than 10 or more than 35. - Severe agitation or seizures on admission. - Obvious loss of airway protective reflexes and/or vomiting on admission. - Being intubated before treatment on admission. - Known allergy to anesthetic or analgesic.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Intravenous anesthetics

local anesthesia

Controlled ventilation

Spontaneous breathing


Locations

Country Name City State
China Beijing TianTan Hospital Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing Tiantan Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary modified Rankin score post-procedural 30 days
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