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Normobaric Hyperoxia Combined With Endovascular Treatment in Acute Ischemic Stroke (OPENS-2)

Primary Purpose

Stroke, Acute, Neuroprotection

Status
Completed
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Normobaric Hyperoxia
Sham Normobaric Hyperoxia
Endovascular Thrombectomy
Sponsored by
Capital Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke, Acute focused on measuring Normobaric hyperoxia, Endovascular treatment, Acute ischemic stroke

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

General inclusion criteria

  1. It conforms to the indications for endovascular thrombectomy
  2. 18 ≦ Age ≦ 80 years old.
  3. The clinical symptoms and signs are consistent with acute anterior circulation large vessel occlusion; 10≤NIHSS≤20;
  4. (Level of consciousness) NIHSS score 0 or 1;
  5. The time from onset to randomization is within 6 hours of onset;
  6. The mRS score before stroke is 0-1;
  7. Patient and family members sign informed consent. Image inclusion criteria

1. Preoperative CT or MR or DSA angiography found large vessel occlusion (internal carotid artery or middle cerebral artery M1 segment) that were consistent with symptoms and signs; 2. ASPECT score ≥ 6 points 3. <1/3 MCA area involvement (confirmed by CT or MRI)

Exclusion Criteria:

  • General exclusion criteria

    1. Rapid neurological function improvement, NIHSS score less than 10 points, or evidence of vessel recanalization prior to randomization;
    2. Seizures at stroke onset;
    3. Intracranial hemorrhage;
    4. Symptoms suggestive of subarachnoid hemorrhage, even if CT scan was normal;
    5. Known hemorrhagic diathesis, coagulation factor deficiency, or on anticoagulant therapy with INR > 3.0 or PTT > 3 times normal;
    6. Platelet count of less than 100,000 per cubic millimeter;
    7. Severe hepatic or renal dysfunction;
    8. Severe, sustained hypertension (Systolic Blood Pressure >185 mmHg or Diastolic Blood Pressure >110 mmHg)
    9. Baseline blood glucose of <50mg/dL (2.78 mmol) or >400mg/dL (22.20 mmol)
    10. Active and chronic obstructive pulmonary disease or acute respiratory distress syndrome;
    11. >3 L/min oxygen required to maintain peripheral arterial oxygen saturation (SaO2) 95% as per current stroke management guidelines;
    12. Medically unstable;
    13. Life expectancy<90 days;
    14. Patients who could not complete the 90-day follow-up;
    15. Evidence of intracranial tumor;
    16. Patients with anemia or polycythemia vera or other situations that require urgent oxygen inhalation;
    17. Patients with upper gastrointestinal bleeding or nausea or vomiting so that they cannot cooperate with the mask to inhale oxygen.
    18. A history of severe allergies to contrast agents;
    19. There are any other conditions that are not suitable for endovascular treatment.

Image exclusion criteria

  1. CTA/MRAshows excessive bending of blood vessels, which may hinder the delivery of the device;
  2. Suspected cerebrovascular inflammation based on medical history and CTA/MRA;
  3. Suspected aortic dissection based on medical history and CTA/MRA
  4. CTA/MRA confirmed multi-vascular area occlusion (such as bilateral anterior circulation or anterior/posterior circulation), or bilateral infarction or multi- regional infarction;
  5. CTA/MRAconfirmed moyamoya disease or moyamoya syndrome;
  6. CT/MRI confirmed the obvious effect of midline shift
  7. CT/MRI confirmed the presence of intracranial tumors

Sites / Locations

  • Xuan Wu Hospital,Capital Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

NBO group

Control group

Arm Description

Normobaric Hyperoxia combined with endovascular mechanical thrombectomy

Inhale air placebo plus endovascular mechanical thrombectomy

Outcomes

Primary Outcome Measures

Modified Rankin Scale (mRS) score
the mRs is an ordinal disability score of 7 categories (0=no symptoms to 5=severe disability, and 6=death)

Secondary Outcome Measures

Cerebral infarct volume
The infarct volume of cerebral infarct is evaluated by MRI or CT
The proportion of good prognosis
defined by mRS 0-2
The proportion of functional independence
defined by mRS 0-1
The proportion of severe disability
defined by mRS 4-6
Scores assessed by National Institutes of Health Stroke Scale(NIHSS)
Scores on the National Institutes of Health Stroke Scale (NIHSS) range from 0 to 42, with higher scores indicating more severe neurologic deficits
The proportion of neurological function improvement
≥ 4 point reduction in NIHSS score from baseline
Successful vessel recanalization
Successful vessel recanalization is defined by eTICI 2b/2c/3 on final angiogram. Extended treatment in cerebral ischaemia (eTICI) score range from 0 to 3, with higher scores indicating better reperfusion
Vessel recanalization
Vessel recanalization is evaluated by CTA or MRA and assessed by AOL grades. Arterial Occlusive Lesion (AOL) range from 0 to 3, with higher scores indicating better recanalization
Arterial oxygen partial pressure
Laboratory indicators, obtained by arterial blood gas analysis
Barthel Index (BI)
the BI is an ordinal disability score of 10 categories (range from 0 to 100, higher values indicate better prognosis)
EuroQol five dimensions questionnaire(EQ-5D)
The score ranges from 0 to 100, with higher scores indicating optimal health
Days of hospitalization
Length of stay in hospital
All-cause mortality
Safety endpoint; the proportion of all patients who died in each group
Serious adverse events
Safety endpoint; the proportion of serious adverse events in each group
Stroke-related mortality
Safety endpoint; the proportion of stroke related deaths in each group
Oxygen-related adverse events
Safety endpoint; the proportion of oxygen-related adverse events in each group, including severe lung infection, pneumothorax, atelectasis, respiratory failure, acute respiratory distress syndrome, and cardiopulmonary arrest
Adverse events of special interest
Safety endpoint; the proportion of adverse events of special interest in each group, including malignant brain edema, perioperative myocardial infarction, and acute heart failure
Symptomatic intracranial hemorrhage
Safety endpoint; according to ECASS II definition
Any intracranial hemorrhage
Safety endpoint; the proportion of any intracranial hemorrhage in each group
Early neurological deterioration (END)
Safety endpoint; defined as ≥4 point increase in NIHSS score from baseline
Systolic and diastolic blood pressure
Safety endpoint; vital signs
Heart rate
Safety endpoint; vital signs
Respiratory rate
Safety endpoint; vital signs
Oxygen saturation
Safety endpoint; vital signs
PH of arterial blood gas analysis
Safety endpoint
PaCO2 of arterial blood gas analysis
Safety endpoint
Lactic acid of arterial blood gas analysis
Safety endpoint

Full Information

First Posted
December 6, 2020
Last Updated
July 4, 2023
Sponsor
Capital Medical University
Collaborators
Tianjin Huanhu Hospital, Shengli Oilfield Hospital, Beijing Fengtai You'anmen Hospital, Jiujiang University Affiliated Hospital, Zhangzhou Municipal Hospital of Fujian Province, Baotou Central Hospital, Luoyang Central Hospital, Nanyang Central Hospital, Qingdao Central Hospital, The Third People's Hospital of Jinan, Rizhao People's Hospital, Anyang People's Hospital, Shanghai 10th People's Hospital, Dalian Municipal Central Hospital, Zhoukou Central Hospital, Nanshi Hospital of Nanyang, The second Nanning People's Hospital, Zhumadian Central Hospital, Taizhou Hospital, Second Affiliated Hospital of Nanchang University
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1. Study Identification

Unique Protocol Identification Number
NCT04681651
Brief Title
Normobaric Hyperoxia Combined With Endovascular Treatment in Acute Ischemic Stroke (OPENS-2)
Official Title
A Randomized Controlled Trial Assessing the Efficacy and Safety of Normobaric Hyperoxia for Acute Ischemic Stroke Patients Undergoing Endovascular Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
April 22, 2021 (Actual)
Primary Completion Date
May 5, 2023 (Actual)
Study Completion Date
May 5, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Capital Medical University
Collaborators
Tianjin Huanhu Hospital, Shengli Oilfield Hospital, Beijing Fengtai You'anmen Hospital, Jiujiang University Affiliated Hospital, Zhangzhou Municipal Hospital of Fujian Province, Baotou Central Hospital, Luoyang Central Hospital, Nanyang Central Hospital, Qingdao Central Hospital, The Third People's Hospital of Jinan, Rizhao People's Hospital, Anyang People's Hospital, Shanghai 10th People's Hospital, Dalian Municipal Central Hospital, Zhoukou Central Hospital, Nanshi Hospital of Nanyang, The second Nanning People's Hospital, Zhumadian Central Hospital, Taizhou Hospital, Second Affiliated Hospital of Nanchang University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The current endovascular treatment has increased the recanalization rate to more than 90%. Even so, the prognosis rate of stroke is still less than 50%. Our previous research confirmed that the neuroprotective effect of Normobaric Hyperoxia (NBO) from multiple perspectives. However, the clinical study on NBO was not satisfactory, which might be due to the absence of vascular recanalization therapy. Therefore, The investigators conducted this RCT study to further explore the Efficacy and safety of NBO combined with endovascular treatment in patients with acute ischemic stroke.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Acute, Neuroprotection
Keywords
Normobaric hyperoxia, Endovascular treatment, Acute ischemic stroke

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
282 (Actual)

8. Arms, Groups, and Interventions

Arm Title
NBO group
Arm Type
Experimental
Arm Description
Normobaric Hyperoxia combined with endovascular mechanical thrombectomy
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
Inhale air placebo plus endovascular mechanical thrombectomy
Intervention Type
Drug
Intervention Name(s)
Normobaric Hyperoxia
Other Intervention Name(s)
NBO
Intervention Description
Within 6 hours after stroke onset, patients were randomized into the NBO group and immediately given 100% oxygen inhalation (no more than 30 minutes after randomization) at a ventilation rate of 10L/ min using a sealed non-ventilating oxygen storage mask and keep giving oxygen for 4 hours. If the patient needs to be intubated with a ventilator to maintain ventilation, the FiO2 should be set to 1.0.
Intervention Type
Drug
Intervention Name(s)
Sham Normobaric Hyperoxia
Other Intervention Name(s)
Sham NBO
Intervention Description
For Sham NBO group, Patients were immediately given oxygen inhalation (no more than 30 minutes after randomization) at a ventilation rate of 1l/min using the same mask and keep giving oxygen for 4 hours. If the patient needs to be intubated with a ventilator to maintain, the FiO2 should be set to 0.3 and gradualy incerased if spO2≤94%;
Intervention Type
Procedure
Intervention Name(s)
Endovascular Thrombectomy
Other Intervention Name(s)
EVT
Intervention Description
EVT is the international guidelines for the treatment of acute ischemic stroke with lage vessel occlusion.
Primary Outcome Measure Information:
Title
Modified Rankin Scale (mRS) score
Description
the mRs is an ordinal disability score of 7 categories (0=no symptoms to 5=severe disability, and 6=death)
Time Frame
90 ± 14 days after randomization
Secondary Outcome Measure Information:
Title
Cerebral infarct volume
Description
The infarct volume of cerebral infarct is evaluated by MRI or CT
Time Frame
24-48h after randomization
Title
The proportion of good prognosis
Description
defined by mRS 0-2
Time Frame
90 ± 14 days after randomization
Title
The proportion of functional independence
Description
defined by mRS 0-1
Time Frame
90 ± 14 days after randomization
Title
The proportion of severe disability
Description
defined by mRS 4-6
Time Frame
90 ± 14 days after randomization
Title
Scores assessed by National Institutes of Health Stroke Scale(NIHSS)
Description
Scores on the National Institutes of Health Stroke Scale (NIHSS) range from 0 to 42, with higher scores indicating more severe neurologic deficits
Time Frame
24 ± 6 hours, 72 ± 24 hours, 7 ± 2 days after randomization
Title
The proportion of neurological function improvement
Description
≥ 4 point reduction in NIHSS score from baseline
Time Frame
24 ± 6 hours after randomization
Title
Successful vessel recanalization
Description
Successful vessel recanalization is defined by eTICI 2b/2c/3 on final angiogram. Extended treatment in cerebral ischaemia (eTICI) score range from 0 to 3, with higher scores indicating better reperfusion
Time Frame
Immediately after procedure
Title
Vessel recanalization
Description
Vessel recanalization is evaluated by CTA or MRA and assessed by AOL grades. Arterial Occlusive Lesion (AOL) range from 0 to 3, with higher scores indicating better recanalization
Time Frame
24 ± 6 hours after randomization
Title
Arterial oxygen partial pressure
Description
Laboratory indicators, obtained by arterial blood gas analysis
Time Frame
after 4 hours of oxygen therapy
Title
Barthel Index (BI)
Description
the BI is an ordinal disability score of 10 categories (range from 0 to 100, higher values indicate better prognosis)
Time Frame
90 ± 14 days after randomization
Title
EuroQol five dimensions questionnaire(EQ-5D)
Description
The score ranges from 0 to 100, with higher scores indicating optimal health
Time Frame
90 ± 14 days after randomization
Title
Days of hospitalization
Description
Length of stay in hospital
Time Frame
90 ± 14 days after randomization
Title
All-cause mortality
Description
Safety endpoint; the proportion of all patients who died in each group
Time Frame
90 ± 14 days after randomization
Title
Serious adverse events
Description
Safety endpoint; the proportion of serious adverse events in each group
Time Frame
90 ± 14 days after randomization
Title
Stroke-related mortality
Description
Safety endpoint; the proportion of stroke related deaths in each group
Time Frame
90 ± 14 days after randomization
Title
Oxygen-related adverse events
Description
Safety endpoint; the proportion of oxygen-related adverse events in each group, including severe lung infection, pneumothorax, atelectasis, respiratory failure, acute respiratory distress syndrome, and cardiopulmonary arrest
Time Frame
90 ± 14 days after randomization
Title
Adverse events of special interest
Description
Safety endpoint; the proportion of adverse events of special interest in each group, including malignant brain edema, perioperative myocardial infarction, and acute heart failure
Time Frame
90 ± 14 days after randomization
Title
Symptomatic intracranial hemorrhage
Description
Safety endpoint; according to ECASS II definition
Time Frame
24 ± 6 hours after randomization
Title
Any intracranial hemorrhage
Description
Safety endpoint; the proportion of any intracranial hemorrhage in each group
Time Frame
24 ± 6 hours after randomization
Title
Early neurological deterioration (END)
Description
Safety endpoint; defined as ≥4 point increase in NIHSS score from baseline
Time Frame
24 ± 6 hours after randomization
Title
Systolic and diastolic blood pressure
Description
Safety endpoint; vital signs
Time Frame
24 ± 6 hours after randomization
Title
Heart rate
Description
Safety endpoint; vital signs
Time Frame
24 ± 6 hours after randomization
Title
Respiratory rate
Description
Safety endpoint; vital signs
Time Frame
24 ± 6 hours after randomization
Title
Oxygen saturation
Description
Safety endpoint; vital signs
Time Frame
24 ± 6 hours after randomization
Title
PH of arterial blood gas analysis
Description
Safety endpoint
Time Frame
after 4 hours of oxygen therapy
Title
PaCO2 of arterial blood gas analysis
Description
Safety endpoint
Time Frame
after 4 hours of oxygen therapy
Title
Lactic acid of arterial blood gas analysis
Description
Safety endpoint
Time Frame
after 4 hours of oxygen therapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: General inclusion criteria It conforms to the indications for endovascular thrombectomy 18 ≦ Age ≦ 80 years old. The clinical symptoms and signs are consistent with acute anterior circulation large vessel occlusion; 10≤NIHSS≤20; (Level of consciousness) NIHSS score 0 or 1; The time from onset to randomization is within 6 hours of onset; The mRS score before stroke is 0-1; Patient and family members sign informed consent. Image inclusion criteria 1. Preoperative CT or MR or DSA angiography found large vessel occlusion (internal carotid artery or middle cerebral artery M1 segment) that were consistent with symptoms and signs; 2. ASPECT score ≥ 6 points 3. <1/3 MCA area involvement (confirmed by CT or MRI) Exclusion Criteria: General exclusion criteria Rapid neurological function improvement, NIHSS score less than 10 points, or evidence of vessel recanalization prior to randomization; Seizures at stroke onset; Intracranial hemorrhage; Symptoms suggestive of subarachnoid hemorrhage, even if CT scan was normal; Known hemorrhagic diathesis, coagulation factor deficiency, or on anticoagulant therapy with INR > 3.0 or PTT > 3 times normal; Platelet count of less than 100,000 per cubic millimeter; Severe hepatic or renal dysfunction; Severe, sustained hypertension (Systolic Blood Pressure >185 mmHg or Diastolic Blood Pressure >110 mmHg) Baseline blood glucose of <50mg/dL (2.78 mmol) or >400mg/dL (22.20 mmol) Active and chronic obstructive pulmonary disease or acute respiratory distress syndrome; >3 L/min oxygen required to maintain peripheral arterial oxygen saturation (SaO2) 95% as per current stroke management guidelines; Medically unstable; Life expectancy<90 days; Patients who could not complete the 90-day follow-up; Evidence of intracranial tumor; Patients with anemia or polycythemia vera or other situations that require urgent oxygen inhalation; Patients with upper gastrointestinal bleeding or nausea or vomiting so that they cannot cooperate with the mask to inhale oxygen. A history of severe allergies to contrast agents; There are any other conditions that are not suitable for endovascular treatment. Image exclusion criteria CTA/MRAshows excessive bending of blood vessels, which may hinder the delivery of the device; Suspected cerebrovascular inflammation based on medical history and CTA/MRA; Suspected aortic dissection based on medical history and CTA/MRA CTA/MRA confirmed multi-vascular area occlusion (such as bilateral anterior circulation or anterior/posterior circulation), or bilateral infarction or multi- regional infarction; CTA/MRAconfirmed moyamoya disease or moyamoya syndrome; CT/MRI confirmed the obvious effect of midline shift CT/MRI confirmed the presence of intracranial tumors
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xunming Ji, MD,PhD
Organizational Affiliation
Capital Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Xuan Wu Hospital,Capital Medical University
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100069
Country
China

12. IPD Sharing Statement

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Normobaric Hyperoxia Combined With Endovascular Treatment in Acute Ischemic Stroke (OPENS-2)

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