A Prospective Study of Vasopressor on Cerebral Oxygenation During General Anesthesia

Recruiting Phase 4 Interventional Study
Hypotension Drug-Induced
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 80
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
180 (estimated)
Sponsor
Dalian Municipal Central Hospital · Other
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About This Trial

The purpose of this study is to investigate whether norepinephrine(N), phenylephrine(P) or ephedrine(E) have different effect on cerebral oxygenation in abdominal surgery with propofol or sevoflurane.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * ASA I-III, age 18-80 years * Elective abdominal surgery * Signed informed consent Exclusion Criteria: * ASA≥IV * Preoperative unstable blood hemodynamics * Allergy to ephedrine, phenylephrine or norepinephrine * Decrease in MAP \<20% * Severe cardiovascular disorder
Contacts

Liping Han, MD, MSc

86-411-84412001

han651310@163.com

CONTACT