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Effects of Remote Ischemic Pre-Conditioning in Moyamoya Disease Patients (RIME)

Primary Purpose

Moyamoya Disease, Remote Ischemic Preconditioning

Status
Suspended
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Remote ischemic preconditioning
Sham remote ischemic preconditioning
Encephaloduroarteriosynangiosis
Sponsored by
Beijing Tiantan Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Moyamoya Disease focused on measuring Moyamoya Disease, Cerebrovascular Disorders, Arterial Occlusive Diseases, Ischemia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Beijing Tiantan Hosiptal
  • Peking University International Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Experimental

Arm Label

Sham RIPC group

RIPC group

Arm Description

Treatment:Patients in this group received standard medical therapy and sham remote ischemic preconditioning treatment. Device:Sham RIPC 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, each patient in Sham RIPC group do it twice a day for at least five days before encephaloduroarteriosynangiosis. Procedure: Encephaloduroarteriosynangiosis

Treatment:Patients in this group received standard medical therapy and remote ischemic preconditioning (RIPC) treatment. Device:RIPC 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,each patient in the RIPC group do it twice a day for at least five days before encephaloduroarteriosynangiosis. Procedure: Encephaloduroarteriosynangiosis

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

The Severity of the Ischemic Stroke after Surgery
The 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 Occured Re-stroke at Follow-up Period
Re-stroke included ischemic stroke and hemorrhagic stroke.
Number of Patients Dependent or Death at Follow-up Period
Dependent included the modified Rankin Scale (mRS) > 2. Death included any reason caused death.
Number of Patients with Improved Neurological Function at Follow-up Period
The modified Rankin Scale (mRS) decreased at the follow-up period compared to preoperative scores
Perfusion Status of Patients at Follow-up Period
The perfusion status detected by stages of pre-infarction period based on computed tomography perfusion imaging
Number of Patients With Any Side Effects of Remote Ischemic Preconditioning (RIPC) Treatment.
The 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.
The presence of ≥1 new brain lesions on DWI

Full Information

First Posted
August 20, 2019
Last Updated
September 17, 2019
Sponsor
Beijing Tiantan Hospital
Collaborators
Peking University International Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04064658
Brief Title
Effects of Remote Ischemic Pre-Conditioning in Moyamoya Disease Patients
Acronym
RIME
Official Title
Effects of Remote Ischemic Pre-Conditioning on Neurologic Complications in Adult Ischemic Moyamoya Disease Patients Undergoing Encephaloduroarteriosynangiosis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Suspended
Why Stopped
waiting for the ethics approval of collaborator affiliation
Study Start Date
October 1, 2019 (Anticipated)
Primary Completion Date
October 1, 2023 (Anticipated)
Study Completion Date
April 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beijing Tiantan Hospital
Collaborators
Peking University International Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Moyamoya Disease, Remote Ischemic Preconditioning
Keywords
Moyamoya Disease, Cerebrovascular Disorders, Arterial Occlusive Diseases, Ischemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
328 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sham RIPC group
Arm Type
Sham Comparator
Arm Description
Treatment:Patients in this group received standard medical therapy and sham remote ischemic preconditioning treatment. Device:Sham RIPC 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, each patient in Sham RIPC group do it twice a day for at least five days before encephaloduroarteriosynangiosis. Procedure: Encephaloduroarteriosynangiosis
Arm Title
RIPC group
Arm Type
Experimental
Arm Description
Treatment:Patients in this group received standard medical therapy and remote ischemic preconditioning (RIPC) treatment. Device:RIPC 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,each patient in the RIPC group do it twice a day for at least five days before encephaloduroarteriosynangiosis. Procedure: Encephaloduroarteriosynangiosis
Intervention Type
Procedure
Intervention Name(s)
Remote ischemic preconditioning
Other Intervention Name(s)
RIPC
Intervention Description
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.
Intervention Type
Procedure
Intervention Name(s)
Sham remote ischemic preconditioning
Other Intervention Name(s)
Sham RIPC
Intervention Description
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.
Intervention Type
Procedure
Intervention Name(s)
Encephaloduroarteriosynangiosis
Other Intervention Name(s)
EDAS
Intervention Description
Encephaloduroarteriosynangiosis is an indirect revascularization surgery of moyamoya disease
Primary Outcome Measure Information:
Title
Number of Patients With Cerebrovascular Events.
Description
Cerebrovascular events included ischemic stroke, transient ischemic attack (TIA), cerebral hemorrhage and hyperperfusion syndrome.
Time Frame
postoperative one month
Title
Number of Patients Dependent or Death
Description
Dependent included the modified Rankin Scale (mRS) > 2. Death included any reason caused death.
Time Frame
postoperative one month
Secondary Outcome Measure Information:
Title
The Severity of the Ischemic Stroke after Surgery
Description
The 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.
Time Frame
postoperative one month
Title
Number of Patients Occured Re-stroke at Follow-up Period
Description
Re-stroke included ischemic stroke and hemorrhagic stroke.
Time Frame
6 months and 12 months after EDAS
Title
Number of Patients Dependent or Death at Follow-up Period
Description
Dependent included the modified Rankin Scale (mRS) > 2. Death included any reason caused death.
Time Frame
6 months and 12 months after EDAS
Title
Number of Patients with Improved Neurological Function at Follow-up Period
Description
The modified Rankin Scale (mRS) decreased at the follow-up period compared to preoperative scores
Time Frame
6 months and 12 months after EDAS
Title
Perfusion Status of Patients at Follow-up Period
Description
The perfusion status detected by stages of pre-infarction period based on computed tomography perfusion imaging
Time Frame
6 months and 12 months after EDAS
Title
Number of Patients With Any Side Effects of Remote Ischemic Preconditioning (RIPC) Treatment.
Description
The side effects referred to any side effects of RIPC or sham RIPC treatment, not including the sides effect of medications and EDAS.
Time Frame
From baseline to 12 months after treatment
Title
Participants Who Got New Diffusion-weighted Imaging (DWI) Lesions on Post-treatment Magnetic Resonance Imaging (MRI) Scans.
Description
The presence of ≥1 new brain lesions on DWI
Time Frame
Within 48 hours after EDAS

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients who diagnosed with moyamoya disease Adults 18 to 65 years of age The onset symptoms manifested as ischemic symptoms (TIA or stroke) or atypical symptoms (headache, epilepsy or asymptomatic) Able to receive the necessary imaging examination Patients who pre-agreed to the study Exclusion Criteria: Prior cerebral hemorrhage history Other brain or cerebrovascular disease Previous history of revascularization surgery Dependent (mRS > 2) Receive other type of revascularization surgery Peripheral blood vessel disease (especially subclavian arterial and upper limb artery stenosis or occlusion). Patients who do not agree with the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yuanli Zhao, MD
Organizational Affiliation
Beijing Tiantan Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rong Wang, MD
Organizational Affiliation
Beijing Tiantan Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beijing Tiantan Hosiptal
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100070
Country
China
Facility Name
Peking University International Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
102206
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The individual participant data (IPD) of this study are available from the principal investigator upon reasonable request.
IPD Sharing Time Frame
6 months after the study ended
IPD Sharing Access Criteria
The IPD of this study are available from the principal investigator upon reasonable request.

Learn more about this trial

Effects of Remote Ischemic Pre-Conditioning in Moyamoya Disease Patients

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