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The Neuroprotection Effect of Dexmedetomidine

The Anti-inflammatory Effect and Hemodynamic Stability of Dexmedetomidine in Aneurysmal Clipping Operation; Compare With Propofol

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03927963
Enrollment
70
Registered
2019-04-25
Start date
2019-05-01
Completion date
2021-02-28
Last updated
2019-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dexmedetomidine

Brief summary

The brain protection effect of dexmedetomidine has been approved in several studies. Basically, the anti-inflammatory effects and reducing catecholamines are thought to be a main role of the protection effect. In many studies reported the advantage of dexmedetomidine as a substitution of other sedative drugs for anesthesia. The anesthesia of intra-cranial aneurysmal clipping operation commonly use intravenous anesthetic agents combined with inhalation anesthesia for neuroprotection, and mostly propofol is used. The aim of this study is to examine the effects of dexmedetomidine on serum inflammatory markers and research the hemodynamic stability of dexmedetomidine compared to propofol in aneurysmal clipping operation.

Interventions

DRUGDexmedetomidine

Dexmedetomidine 0.7 ug/kg/h with sevoflurane 0.5 MAC and remifentanil infusion are used throughout anesthesia period

DRUGPropofol

Effect site concentration of propofol 1.5 ng/ml with sevoflurane 0.5 MAC and remifentanil infusion are used throughout anesthesia period

Sponsors

Ajou University School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* ASA class I,II patient needs operation of intracranial aneurysmal clipping without SAH

Exclusion criteria

* Any history of neurologic disease, dementia * Allergic history of propofol or dexmedetomidine

Design outcomes

Primary

MeasureTime frameDescription
The concentration of inflammatory markersBaseline: Before injection study drugsCRP (mg/ml)
The concentration of norepinephrineBaseline: Before injection study drugsNE (nmol/l)

Secondary

MeasureTime frame
The frequency of hypotension or hypertensionduring operation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026