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Effects of Remote Ischemic Pre-Conditioning in Moyamoya Disease Patients

Effects of Remote Ischemic Pre-Conditioning on Neurologic Complications in Adult Ischemic Moyamoya Disease Patients Undergoing Encephaloduroarteriosynangiosis

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04064658
Acronym
RIME
Enrollment
328
Registered
2019-08-22
Start date
2019-10-01
Completion date
2024-04-01
Last updated
2019-09-19

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

Conditions

Moyamoya Disease, Remote Ischemic Preconditioning

Keywords

Moyamoya Disease, Cerebrovascular Disorders, Arterial Occlusive Diseases, Ischemia

Brief summary

In the present study, investigators evaluated whether RIPC reduce the major neurological complications in adult moyamoya disease patients undergoing encephaloduroarteriosynangiosis (EDAS).

Detailed description

BACKGROUND: Brain ischemia and injury contributed to perioperative morbidity and mortality in revascularization surgery. Remote ischemic preconditioning (RIPC), brief periods of ischemia followed by reperfusion, can provide systemic protection for prolonged ischemia. Previous study found combined remote ischemic pre- and post-conditioning can be effective in reducing neurologic complications and the duration of hospitalization in moyamoya patients undergoing direct revascularization.In order to investigate whether RIPC before EDAS can protect these patients from the perioperative and long-term complications, a prospective randomized controlled trial will be performed in the current study. DESIGNING: About 328 patients who are eligible for carotid artery stenting will be randomly assigned in 1:1 ratio to RIPC group and sham RIPC group (control). Remote limb ischemic preconditioning (RIPC) is consisted of five 5-min cycles of bilateral arm ischemia/reperfusion, it is induced by a sphygmomanometer placed on bilateral arm and inflated to 200 mmHg for 5-min followed by deflating the cuff for 5-min, patients in the RIPC group will do it twice a day for at least five days before EDAS. Patients in the sham RIPC group receive sham RIPC treatment, which is consisted of five 5-min cycles of bilateral arm ischemia/reperfusion, induced by a sphygmomanometer placed on bilateral arm and inflated to 60 mmHg for 5-min followed by deflating the cuff for 5-min, they will do it twice a day for at least five days before EDAS. Cerebral injury is assessed by plasma Human Soluble protein-100B (S-100B) and Neuron specific enolase (NSE). Clinical outcomes are determined by cerebrovascular events (including ischemic stroke, transient ischemic attack (TIA), cerebral hemorrhage and transient neurological deficit) and death or dependent.

Interventions

PROCEDURERemote ischemic preconditioning

Remote ischemic preconditioning consisted of five 5-min cycles of bilateral arm ischemia/reperfusion, which is induced by a sphygmomanometer placed on bilateral arm and inflated to 200 mmHg for 5-min followed by deflating the cuff for 5-min.

Sham remote ischemic preconditioning consisted of five 5-min cycles of bilateral arm ischemia/reperfusion, which is induced by a sphygmomanometer placed on bilateral arm and inflated to 60 mmHg for 5-min followed by deflating the cuff for 5-min.

PROCEDUREEncephaloduroarteriosynangiosis

Encephaloduroarteriosynangiosis is an indirect revascularization surgery of moyamoya disease

Sponsors

Peking University International Hospital
CollaboratorOTHER
Beijing Tiantan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Patients who diagnosed with moyamoya disease 2. Adults 18 to 65 years of age 3. The onset symptoms manifested as ischemic symptoms (TIA or stroke) or atypical symptoms (headache, epilepsy or asymptomatic) 4. Able to receive the necessary imaging examination 5. Patients who pre-agreed to the study

Exclusion criteria

1. Prior cerebral hemorrhage history 2. Other brain or cerebrovascular disease 3. Previous history of revascularization surgery 4. Dependent (mRS \> 2) 5. Receive other type of revascularization surgery 6. Peripheral blood vessel disease (especially subclavian arterial and upper limb artery stenosis or occlusion). 7. Patients who do not agree with the study

Design outcomes

Primary

MeasureTime frameDescription
Number of Patients With Cerebrovascular Events.postoperative one monthCerebrovascular events included ischemic stroke, transient ischemic attack (TIA), cerebral hemorrhage and hyperperfusion syndrome.
Number of Patients Dependent or Deathpostoperative one monthDependent included the modified Rankin Scale (mRS) \> 2. Death included any reason caused death.

Secondary

MeasureTime frameDescription
Number of Patients Dependent or Death at Follow-up Period6 months and 12 months after EDASDependent included the modified Rankin Scale (mRS) \> 2. Death included any reason caused death.
Number of Patients with Improved Neurological Function at Follow-up Period6 months and 12 months after EDASThe modified Rankin Scale (mRS) decreased at the follow-up period compared to preoperative scores
The Severity of the Ischemic Stroke after Surgerypostoperative one monthThe severity of the ischemic stroke was evaluated by the white matter hyperintensities volume on the MRI, the neurological deficits duration and the Modified Rankin Scale (mRS) of patients.
Number of Patients With Any Side Effects of Remote Ischemic Preconditioning (RIPC) Treatment.From baseline to 12 months after treatmentThe side effects referred to any side effects of RIPC or sham RIPC treatment, not including the sides effect of medications and EDAS.
Participants Who Got New Diffusion-weighted Imaging (DWI) Lesions on Post-treatment Magnetic Resonance Imaging (MRI) Scans.Within 48 hours after EDASThe presence of ≥1 new brain lesions on DWI
Perfusion Status of Patients at Follow-up Period6 months and 12 months after EDASThe perfusion status detected by stages of pre-infarction period based on computed tomography perfusion imaging
Number of Patients Occured Re-stroke at Follow-up Period6 months and 12 months after EDASRe-stroke included ischemic stroke and hemorrhagic stroke.

Countries

China

Outcome results

None listed

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