CClinicalTrials.gg
Status unknownNCT01204268Updated Sep 20, 2010

The Neuroprotection of Sevoflurane Preconditioning on Intracranial Aneurysm Surgery

An interventional study of Sev-I group and Sevo continuous inhalation in Brain Ischemia, sponsored by Xijing Hospital. Status unknown at 1 site in China. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2010-09-20.

Sponsored by Xijing Hospital · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Aug 2009), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

The current study is designed to clarify the neuroprotective effect of sevoflurane preconditioning on the patients underwent intracranial aneurysm surgery.

Read the detailed description

The current study is designed to clarify the neuroprotective effect of sevoflurane preconditioning on the patients underwent intracranial aneurysm surgery. The patients with cerebral aneurysm will be recruited in current study. The sevoflurane preconditioning will be performed before the surgical procedure. The neurological injury biomarkers, such as S-100b and NSE will be detected. The neurological function and recovery will be assessed after the surgery.

02

Conditions studied

  • Brain Ischemia

Keywords

  • cerebral ischemia
  • sevoflurane preconditioning
  • intracranial aneurysm surgery
03

In context

Intracranial Aneurysm

427 studies on the registry are indexed under Intracranial Aneurysm; 115 are open to participants now.

This study's planned enrollment of 80 is below the median of 110 across 207 interventional studies indexed under Intracranial Aneurysm.

Browse Intracranial Aneurysm studies →

Lead sponsor

Xijing Hospital is the lead sponsor of 465 studies on the registry; 157 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patient under intracranial aneurysm surgery.

Exclusion criteria

Exclusion Criteria:

  • Patients who refused to participate or who had a history of chemotherapy/convulsions two weeks prior to admission, stroke/cardiopulmonary resuscitation/head trauma three months prior to admission, Alzheimer's disease, amyotrophic lateral sclerosis, and prior melanoma were excluded.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
80 participants (estimated)

Study arms

  • No intervention
    Propofol group

    Patients will receive the total intravenous anesthesia with propofol infusion during the surgery.

  • Active comparator
    Sevo-C group

    Patients will receive the anesthesia with continuous inhalation of sevoflurane.

    Procedure: Sevo continuous inhalation

  • Experimental
    Sevo-I group

    Sevoflurane will be given before the cerebral artery clip as a preconditioning procedure for the coming ischemia-reperfusion injury.

    Procedure: Sev-I group

Interventions

  • ProcedureSev-I group

    Sevoflurane will be given before the cerebral artery clip as a preconditioning procedure for the coming ischemia-reperfusion injury.

    Also known as: Sevoflurane preconditioning

  • ProcedureSevo continuous inhalation

    Patients will receive the anesthesia with continuous inhalation of sevoflurane.

06

What researchers measure

Primary outcomes

  1. S-100B,NSE

    Time frame: 7 days

Secondary outcomes

  1. Karnofsky Performance Scale,NIH stroke index, MMSE

    Time frame: 6 months

07

Study locations

1 of 1 sites recruiting
  • Xijing Hospital
    Xi'an, Shaanxi 710032, China
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 20, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01204268
Lead sponsor
Xijing Hospital
First posted
Sep 17, 2010
Start date
Aug 2009
Primary completion
Aug 2011 (estimated)
Completion
Oct 2011 (estimated)
Last update
Sep 20, 2010

Study contacts

Hailong Dong, MD, PhD
principal investigator · Xijing Hospital

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2009. You cannot join it, but the record below documents what was studied.

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