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Outcome in Patients Treated With Intraarterial Thrombectomy - optiMAL Blood Pressure Control (OPTIMAL-BP)

Primary Purpose

Ischemic Stroke

Status
Active
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
conventional blood pressure control (labetalol, nicardipine)
intensive blood pressure control (labetalol, nicardipine)
Sponsored by
Yonsei University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemic Stroke focused on measuring Acute ischemic stroke, blood pressure, hypertension, endovascular thrombectomy, recanalization

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age ≥20 years
  2. Acute ischemic stroke patients who underwent intraarterial treatment for large vessel occlusion. (ICA, MCA M1 or M2, ACA A1, PCA P1)
  3. Patients with successful recanalization after intraarterial thrombectomy (TICI 2b or TICI 3)
  4. Patients with an average blood pressure ≥140 mmHg measured twice within 2 hours of successful recanalization.

Exclusion Criteria:

  1. Age <20
  2. Patients with contraindication for use antihypertensive medication after intraarterial thrombectomy.
  3. Patients with blood pressure <140 mmHg after successful recanalization.
  4. Patients with symptomatic intracranial hemorrhage after successful recanalization
  5. Patients with pre-morbid neurological dysfunction (modified Rankin Scale, mRS >2)
  6. Patients with severe medical and surgical diseases.
  7. Patients who are considered having a difficulty to enrollment.
  8. No informed consents from patients.

Sites / Locations

  • Department of Neurology, Yonsei University College of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Conventional blood pressure control group

Intensive blood pressure control group

Arm Description

systolic blood pressure <180 mmHg

systolic blood pressure <140 mmHg

Outcomes

Primary Outcome Measures

Modified Rankin scale scores(mRS)
Effectiveness outcome: Functional independence (modified Rankin score 0 to 2) -The Modified Rankin Score (mRS) is a 6 point disability scale with possible scores ranging from 0 to 5. A separate category of 6 is usually added for patients who expire.
symptomatic intracerebral hemorrhage: Number of participants with symptomatic intracerebral hemorrhage
Safety outcome: The definition in the European Cooperative Acute Stroke Study III (ECASS 3) will be adopted : a large local or remote parenchymal pattern (>30% of the infarcted area affected by hemorrhage, with mass effect or extension outside the infarct), intraventricular hemorrhage, or subarachnoid hemorrhage which is identified as the predominant cause of the neurologic deterioration from baseline (increase of ≥4 points in the NIHSS score) or death within 36 hours.
Death related to the index stroke within 90 days

Secondary Outcome Measures

BP parameters - systolic blood pressure
change in systolic blood pressure
BP parameters - diastolic blood pressure
change in diastolic blood pressure
BP parameters - blood pressure variability
change in blood pressure variability
Functional independence
modified Rankin score 0 to 2
Distribution of the modified Rankin scores (shift analysis)
The Modified Rankin Score (mRS) is a 6 point disability scale with possible scores ranging from 0 to 5. A separate category of 6 is usually added for patients who expire.
National Institutes of Health Stroke Scale(NIHSS) score
The NIHSS is composed of 11 items, each of which scores a specific ability between a 0 and 4. For each item, a score of 0 typically indicates normal function in that specific ability, while a higher score is indicative of some level of impairment.
Excellent recovery
NIHSS 0 -1 or improvement more than 8. The NIHSS is composed of 11 items, each of which scores a specific ability between a 0 and 4. For each item, a score of 0 typically indicates normal function in that specific ability, while a higher score is indicative of some level of impairment.
Recanalization status on CT Angiography(CTA) or MR Angiography(MRA)
occurence of TICI 2b or 3 recanalization on CTA or MRA - The thrombolysis in cerebral infarction(TICI) scale is a tool for determining the response of thrombolytic therapy for ischemic stroke. The original description 1 was based on the angiographic appearances of the treated occluded vessel and the distal branches(Grade 0: no perfusion, Grade 1: penetration with minimal perfusion, Grade 2: partial perfusion, Grade 2A: only partial filling(less than two-thirds) of the entire vascular territory is visualized, Grade 2B: complete filling of all of the expected vascular territory is visualized but the filling is slower than normal, Grade 3: complete perfusion)
Quality of life measured by Euro-QoL
EuroQol-5D (EQ-5D) is an instrument for measuring quality of life. The answers given to ED-5D permit to find 243 unique health states or can be converted into EQ-5D index an utility scores anchored at 0 for death and 1 for perfect health.
Number of participants with malignant brain edema
1) acute, complete MCA(middle cerebral artery) infarction with early parenchymal hypodensity of at least 50% of the MCA territory and signs of local brain swelling such as sulcal effacement and compression of the lateral ventricle; 2) midline shift of >5 mm at the septum pellucidum or pineal gland with obliteration of the basal cisterns; and 3) neurological deterioration consisting of a NIHSS increase by >2 points and decrease in the level of consciousness to a score of ≥ 1 on item 1A of the NIHSS.
Number of participants with treatment failure
failure to achieve goal blood pressure(BP) for 2 consecutive BP measurements during the first 24 hours following EVT(endovascular thrombectomy)
CT or MRI ASPECTS(Alberta Stroke Program Early CT Score)
Alberta Stroke Program Early CT Score(ASPECTS) is a 10-point quantitative score used to assess early ischemic changes on non-contrast CT head. To compute the ASPECTS, 1 point is subtracted from 10 for any evidence of early ischemic change for each of the defined regions. Identifying patients with a greater likelihood of poor functional outcome (scores <8) may be helpful in the early stages of care for supporting transfer or therapy decisions.

Full Information

First Posted
November 21, 2019
Last Updated
March 29, 2023
Sponsor
Yonsei University
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1. Study Identification

Unique Protocol Identification Number
NCT04205305
Brief Title
Outcome in Patients Treated With Intraarterial Thrombectomy - optiMAL Blood Pressure Control (OPTIMAL-BP)
Official Title
Outcome in Patients Treated With Intraarterial Thrombectomy - optiMAL Blood Pressure Control (OPTIMAL-BP)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 18, 2020 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yonsei University

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
Recent endovascular thrombectomy (EVT) trial have proven the effectiveness of intraarterial revascularization in patients with larger cerebral artery occlusion. The success rate of EVT is close to 80%, but only 50% of patients improve to independent functional outcome. Therefore, new treatment strategies are needed to reduce the futile revascularization. However, updated guidelines recommend the indications for EVT based on the results of randomized clinical trials (RCT), management of post-revascularization is largely unknown. Current guidelines suggest that systolic blood pressure should be adjusted below 180 mmHg and diastolic blood pressure below 105 mmHg in patients undergoing intraarterial reopening. However, in the case of successful recanalization by EVT, same guideline is adopted even though the possibility of intracerebral hemorrhage or reperfusion injury by high blood pressure. On the other hand, too low blood pressure can worsen cerebral ischemia. Therefore, this study will compare the effectiveness of active blood pressure control group (with less than 140 mmHg systolic blood pressure) versus standard blood pressure control group (with less than 180 mmHg systolic blood pressure) during the first 24 hours in patients who underwent EVT and achieved successful recanalization (TICI 2b-3). The goal is to reach the target blood pressure within 60 minutes of randomization.
Detailed Description
The study is a multicenter, prospective, randomized, open-label trial with blinded end-point assessment (PROBE) design study. After successful revascularization, the active blood pressure control group and the standard blood pressure control group will be randomized by 1: 1. Patients who is admitted to the Department of Neurology at the participating hospital with acute cerebral infarction will will be included for 5 years from December 2019 to December 2023 (based on the date of stroke). Patients who have undergone intraarterial thrombectomy and have successfully reopened arteries should be enrolled. Collect medical history, laboratory findings and blood pressure parameters (systolic blood pressure, diastolic blood pressure, blood pressure variability, etc.), neurological scores, functional recovery, and quality of life indicators. Neurological scores, functional recovery scores, and quality of life indicators are performed by independent researchers in the blind state. All data is collected using e-CRF, and the image study will be anonymized and sent to the central adjudication. Central adjudication will review the image study. One intermediate analysis will be conducted at the end of first period or when a half of study patients were enrolled.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Stroke
Keywords
Acute ischemic stroke, blood pressure, hypertension, endovascular thrombectomy, recanalization

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
The study is a multicenter, prospective, randomized, open-label trial with blinded end-point assessment (PROBE) design study. After successful revascularization, the active blood pressure control group and the standard blood pressure control group will be randomized by 1: 1. Patients who have undergone intraarterial thrombectomy due to acute cerebral infarction and have successfully reopened arteries will be enrolled. Medical history, laboratory findings and blood pressure parameters (systolic blood pressure, diastolic blood pressure, blood pressure variability, etc.), neurological scores, functional recovery, and quality of life indicators will be collected. Neurological scores, functional recovery scores, and quality of life indicators are performed by independent researchers in the blind state. All data is collected using e-CRF, and the image study will be anonymized and sent to the central adjudication.
Masking
Outcomes Assessor
Masking Description
Three months after discharge, the independence assessment will be performed by the researcher who don't know the patients group.
Allocation
Randomized
Enrollment
306 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Conventional blood pressure control group
Arm Type
Active Comparator
Arm Description
systolic blood pressure <180 mmHg
Arm Title
Intensive blood pressure control group
Arm Type
Experimental
Arm Description
systolic blood pressure <140 mmHg
Intervention Type
Drug
Intervention Name(s)
conventional blood pressure control (labetalol, nicardipine)
Intervention Description
After successful recanalization, appropriate antihypertension medication is administered to control systolic blood pressure <180 mmHg.
Intervention Type
Drug
Intervention Name(s)
intensive blood pressure control (labetalol, nicardipine)
Intervention Description
After successful recanalization, appropriate antihypertension medication is administered to control systolic blood pressure <140 mmHg.
Primary Outcome Measure Information:
Title
Modified Rankin scale scores(mRS)
Description
Effectiveness outcome: Functional independence (modified Rankin score 0 to 2) -The Modified Rankin Score (mRS) is a 6 point disability scale with possible scores ranging from 0 to 5. A separate category of 6 is usually added for patients who expire.
Time Frame
90 days
Title
symptomatic intracerebral hemorrhage: Number of participants with symptomatic intracerebral hemorrhage
Description
Safety outcome: The definition in the European Cooperative Acute Stroke Study III (ECASS 3) will be adopted : a large local or remote parenchymal pattern (>30% of the infarcted area affected by hemorrhage, with mass effect or extension outside the infarct), intraventricular hemorrhage, or subarachnoid hemorrhage which is identified as the predominant cause of the neurologic deterioration from baseline (increase of ≥4 points in the NIHSS score) or death within 36 hours.
Time Frame
36 hours
Title
Death related to the index stroke within 90 days
Time Frame
90 days
Secondary Outcome Measure Information:
Title
BP parameters - systolic blood pressure
Description
change in systolic blood pressure
Time Frame
24 hour
Title
BP parameters - diastolic blood pressure
Description
change in diastolic blood pressure
Time Frame
24 hour
Title
BP parameters - blood pressure variability
Description
change in blood pressure variability
Time Frame
24 hour
Title
Functional independence
Description
modified Rankin score 0 to 2
Time Frame
1 month
Title
Distribution of the modified Rankin scores (shift analysis)
Description
The Modified Rankin Score (mRS) is a 6 point disability scale with possible scores ranging from 0 to 5. A separate category of 6 is usually added for patients who expire.
Time Frame
90 days
Title
National Institutes of Health Stroke Scale(NIHSS) score
Description
The NIHSS is composed of 11 items, each of which scores a specific ability between a 0 and 4. For each item, a score of 0 typically indicates normal function in that specific ability, while a higher score is indicative of some level of impairment.
Time Frame
24 hour
Title
Excellent recovery
Description
NIHSS 0 -1 or improvement more than 8. The NIHSS is composed of 11 items, each of which scores a specific ability between a 0 and 4. For each item, a score of 0 typically indicates normal function in that specific ability, while a higher score is indicative of some level of impairment.
Time Frame
24 hour
Title
Recanalization status on CT Angiography(CTA) or MR Angiography(MRA)
Description
occurence of TICI 2b or 3 recanalization on CTA or MRA - The thrombolysis in cerebral infarction(TICI) scale is a tool for determining the response of thrombolytic therapy for ischemic stroke. The original description 1 was based on the angiographic appearances of the treated occluded vessel and the distal branches(Grade 0: no perfusion, Grade 1: penetration with minimal perfusion, Grade 2: partial perfusion, Grade 2A: only partial filling(less than two-thirds) of the entire vascular territory is visualized, Grade 2B: complete filling of all of the expected vascular territory is visualized but the filling is slower than normal, Grade 3: complete perfusion)
Time Frame
24±12 hour
Title
Quality of life measured by Euro-QoL
Description
EuroQol-5D (EQ-5D) is an instrument for measuring quality of life. The answers given to ED-5D permit to find 243 unique health states or can be converted into EQ-5D index an utility scores anchored at 0 for death and 1 for perfect health.
Time Frame
90 days
Title
Number of participants with malignant brain edema
Description
1) acute, complete MCA(middle cerebral artery) infarction with early parenchymal hypodensity of at least 50% of the MCA territory and signs of local brain swelling such as sulcal effacement and compression of the lateral ventricle; 2) midline shift of >5 mm at the septum pellucidum or pineal gland with obliteration of the basal cisterns; and 3) neurological deterioration consisting of a NIHSS increase by >2 points and decrease in the level of consciousness to a score of ≥ 1 on item 1A of the NIHSS.
Time Frame
24 hour
Title
Number of participants with treatment failure
Description
failure to achieve goal blood pressure(BP) for 2 consecutive BP measurements during the first 24 hours following EVT(endovascular thrombectomy)
Time Frame
24 hour
Title
CT or MRI ASPECTS(Alberta Stroke Program Early CT Score)
Description
Alberta Stroke Program Early CT Score(ASPECTS) is a 10-point quantitative score used to assess early ischemic changes on non-contrast CT head. To compute the ASPECTS, 1 point is subtracted from 10 for any evidence of early ischemic change for each of the defined regions. Identifying patients with a greater likelihood of poor functional outcome (scores <8) may be helpful in the early stages of care for supporting transfer or therapy decisions.
Time Frame
36 hour

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥20 years Acute ischemic stroke patients who underwent intraarterial treatment for large vessel occlusion. (ICA, MCA M1 or M2, ACA A1, PCA P1) Patients with successful recanalization after intraarterial thrombectomy (TICI 2b or TICI 3) 4. Patients with elevated BP (systolic BP ≥140 mmHg) on at least two measurements with a two-minute interval within 2 hours of successful recanalization. Exclusion Criteria: Age <20 Patients with contraindication for use antihypertensive medication after intraarterial thrombectomy. Patients with blood pressure <140 mmHg after successful recanalization. Patients with symptomatic intracranial hemorrhage after successful recanalization Patients with pre-morbid neurological dysfunction (modified Rankin Scale, mRS >2) Patients with severe medical and surgical diseases. Patients who are considered having a difficulty to enrollment. No informed consents from patients. Patients who participated in a study that did not allow duplicate participation
Facility Information:
Facility Name
Department of Neurology, Yonsei University College of Medicine
City
Seoul
ZIP/Postal Code
120-752
Country
Korea, Republic of

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
This is not a drug comparison study. Therefore IPD will not be shared.
Citations:
PubMed Identifier
34427481
Citation
Nam HS, Kim YD, Choi JK, Baik M, Kim BM, Kim DJ, Heo J, Shin DH, Lee KY, Jung YH, Baek JH, Hwang YH, Sohn SI, Hong JH, Park H, Kim CK, Kim GS, Seo KD, Lee K, Seo JH, Bang OY, Seo WK, Chung JW, Chang JY, Kwon SU, Lee J, Kim J, Yoo J, Song TJ, Ahn SH, Cho BH, Cho HJ, Kim JG, Chang Y, Lee CJ, Park S, Park G, Lee HS. Outcome in Patients Treated with Intra-arterial thrombectomy: The optiMAL Blood Pressure control (OPTIMAL-BP) Trial. Int J Stroke. 2021 Aug 29:17474930211041213. doi: 10.1177/17474930211041213. Online ahead of print.
Results Reference
derived

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Outcome in Patients Treated With Intraarterial Thrombectomy - optiMAL Blood Pressure Control (OPTIMAL-BP)

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