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Sevoflurane and Hyperperfusion Syndrome

Effect of Sevoflurane-induced Postconditioning on the Incidence of Postoperative Cerebral Hyperperfusion Syndrome After Revascularization Surgery in Adult Patients With Moyamoya Disease

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02510586
Enrollment
152
Registered
2015-07-29
Start date
2015-08-31
Completion date
2018-09-30
Last updated
2015-07-29

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

Conditions

Hyperperfusion Syndrome, Moyamoya Disease

Brief summary

The aim of the present study is to evaluate the effect of sevoflurane postconditioning on the incidence of postoperative hyperperfusion syndrome following revascularization surgery in moyamoya patients.

Detailed description

Postoperative hyperperfusion syndrome is a common complication in moyamoya disease patients receiving revascularization surgery. Previously its incidence has been reported to be 17\ 50%, but little remains regarding frequency of reperfusion injury after revascularization surgery in patients with moyamoya disease. Volatile anesthetics such as sevoflurane has been introduced clinically to reduce reperfusion injury and preconditioning with sevoflurane induced ischemic tolerance like as ischemic preconditioning. However, there was no report on the neuroprotective effect of sevoflurane postconditioning on ischemic/reperfusion injury in human brain. Therefore, We evaluated the neuroprotective effect of sevoflurane postconditioning on the incidence of postoperative hyperperfusion syndrome after revascularization surgery in moyamoya disease patients.

Interventions

DRUGSevoflurane

administer 1.0 MAC (1.7\ 2.0 vol%) of sevoflurane for 30 minutes after vascular anastomosis completed

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients receiving cerebral revascularization surgery due to moyamoya disease

Exclusion criteria

* Patients who do not agree to the study * Patients with uncontrolled diabetes or hypertension * Patients using cyclooxygenase2 inhibitor or with previously using cyclooxygenase2 inhibitor * Patients with acute renal failure * Patients with previous intervention related with moyamoya disease

Design outcomes

Primary

MeasureTime frameDescription
The incidence of postoperative cerebral hyperperfusion syndromepostoperative day 15Cerebral hyperperfusion syndrome was defined if all the following four criteria were met: i) new development of postoperative focal neurological deficits, ii) a delayed neurological deficits which were not shown in the immediate postoperative period; iii) postoperative reversible neurological deficits which were completely resolved within 15 days after operation; iii) neither definite haematomas nor definite acute infarction on a brain CT scan, on diffusion magnetic resonance imaging, or both.

Secondary

MeasureTime frameDescription
The incidence of a new onset postoperative cerebral ischemiaparticipants will be followed for the duration of hospital stay, an expected average of 3 weeks.cerebral ischemia is diagnosed by clinical symptoms and radiologic imaging (CT or MRI).
The incidence of a new onset postoperative brain hematomaparticipants will be followed for the duration of hospital stay, an expected average of 3 weeks.postoperative brain hematoma is diagnosed by clinical symptoms and radiologic imaging (CT or MRI).
The incidence of unrecovered neurological deficitparticipants will be followed for the duration of hospital stay, an expected average of 3 weeks.the incidence of postoperative neurological symptoms which persisted or not fully recovered until the patient's discharge.

Contacts

Primary ContactHee Pyung Park, MD, PhD
hppark@snu.ac.kr82-2-2072-2466
Backup ContactHyungseok Seo, MD
seohyungseok@gmail.com82-2-2072-2469

Outcome results

None listed

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