The current study is designed to investigate the difference of plasma orexin A levels between
Dexmedetomidine group and controlled group at emergence time from total intravenous
anesthesia who will undergo elective lumbar surgery.
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Locations near you
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Full eligibility criteria for NCT03025295
Ages eligible for Study
18 Years to 60 Years
Genders eligible for Study
Accepts Healthy Volunteers
Participant is Adult (≥18 years old and ≤60 years old)
Participants with a Body Mass Index (BMI) 20-25 kg/m2
Participants with ASA physical status Ⅰor Ⅱ
Participants with Heart function rating Ⅰor Ⅱ
Patients will undergo elective surgery and general anesthesia
The operation time is 2h to 4h.
Participant is a pregnant woman or a nursing mother.
Participants have a history of narcotics allergic reactions.
Indices of liver or kidney function is twice higher than normal.
Participants have a history or diagnosis of depression.
Participants have a history of Brain Trauma.
Participants have a history of narcotics addiction or drug addiction.
Participants or his family have an International Classification of Sleep
Disorders diagnosis of obstructive sleep apnea syndrome.
Patients are refuse this trail or are not able to sign informed consent.
All locations for NCT03025295
Anesthesiology department of General Hospital of Ningxia Medical University
Yinchuan, Ningxia, China, 750004
View full eligibility
Tris trial is registered with FDA with number: NCT03025295. The sponsor of the trial is General hospital of ningxia medical university and it is looking for 51 volunteers for the current phase.
Official trial title: The Effect of Orexin on Delayed Emergence of General Anesthesia in Dexmedetomidine
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