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Ciprofol vs Propofol for Hemodynamic Stability in Patients Having General Anesthesia for Endovascular Thrombectomy After Ischemic Stroke

2026年7月6日 更新者:RenJi Hospital

Ciprofol vs Propofol for Hemodynamic Stability in Patients Having General Anesthesia for Endovascular Thrombectomy After Ischemic Stroke: A Multicenter Randomized Open-label Parallel-group Trial (CONSTANCY)

Endovascular therapy (EVT) improves the prognosis of patients with acute ischemic stroke (AIS). EVT has been established as a standard of care for AIS caused with large vessel occlusion based on numerous randomized controlled trials. However, despite extensive attention to post-EVT blood pressure management as a potentially modifiable factor, the ability to achieve high reperfusion rates does not consistently translate into functional independence for a substantial number of patients. Thus, the focus has turned to the intra-procedural period, where blood pressure management may play a critical but underexamined role in determining functional outcomes independent of post-EVT care.

Guideline recommendation to maintain the blood pressure lowered to 185/110 mmHg before the EVT procedure in patients who have not received intravenous thrombolysis therapy. However, studies of blood pressure before reperfusion in this patient group have produced conflicting results. Thus, although randomized trials evaluating pre-thrombectomy blood pressure targets are yet unavailable, accumulating evidence suggests that active blood pressure lowering before reperfusion may be harmful, which underscores the importance of maintaining hemodynamic stability during the EVT procedure.

In this context, anesthetic management is a key determinant of intraprocedural blood pressure control. Propofol is the most commonly used general anesthetic during EVT surgery. However, propofol is a powerful venodilator and often provokes hypotension which may be especially detrimental in AIS patients. Ciprofol, a novel anesthetic/sedative, has been proven to possess excellent efficacy and safety which provides definitive general anesthesia/sedation while minimizing respiratory and hemodynamic depression. Before and during EVT, patients with hemodynamic stability may have better outcomes. Using ciprofol as the anesthesia agent may reduce the incidence and severity of hemodynamic instability during EVT. Therefore, it is of significant research value to investigate whether the use of ciprofol for general anesthesia is beneficial in AIS patients undergoing EVT.

調査の概要

状態

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詳細な説明

Endovascular therapy (EVT) improves the prognosis of patients with acute ischemic stroke (AIS). EVT has been established as a standard of care for AIS caused with large vessel occlusion based on numerous randomized controlled trials. However, despite extensive attention to post-EVT blood pressure management as a potentially modifiable factor, the ability to achieve high reperfusion rates does not consistently translate into functional independence for a substantial number of patients. Consequently, post-EVT intensive blood pressure lowering has not been recommended. In fact, the ischemic brain prior to reperfusion may be more vulnerable to blood pressure fluctuations due to disrupted microvascular integrity and impaired autoregulation. Thus, the focus has turned to the intra-procedural period, where blood pressure management may play a critical but underexamined role in determining functional outcomes independent of post-EVT care.

Guideline recommendation to maintain the blood pressure lowered to 185/110 mmHg before the EVT procedure in patients who have not received intravenous thrombolysis therapy is based on expert opinion. However, studies of blood pressure before reperfusion in this patient group have produced conflicting results. Multicenter Randomized Controlled Trial of Endovascular Treatment for Acute Ischemic Stroke in the Netherlands (MR CLEAN) registry showed an increase in systolic blood pressure above 150 mmHg before EVT was associated with poor functional outcome and mortality at 90 days, whereas individual patient data meta-analysis found that admission SBP ≥140 mmHg was associated with worse functional outcome, but no such association was observed for SBP <140 mmHg. Furthermore, subgroup analyses of two randomized controlled trials consistently showed that intensive blood pressure lowering before reperfusion was associated with worse functional outcomes. Thus, although randomized trials evaluating pre-thrombectomy blood pressure targets are yet unavailable, accumulating evidence suggests that active blood pressure lowering before reperfusion may be harmful, which underscores the importance of maintaining hemodynamic stability during the EVT procedure.

In this context, anesthetic management is a key determinant of intraprocedural blood pressure control. Propofol is the most commonly used general anesthetic during EVT surgery. However, propofol is a powerful venodilator and often provokes hypotension which may be especially detrimental in AIS patients. Ciprofol, a novel anesthetic/sedative, has been proven to possess excellent efficacy and safety which provides definitive general anesthesia/sedation while minimizing respiratory and hemodynamic depression. Before and during EVT, patients with hemodynamic stability may have better outcomes. Using ciprofol as the anesthesia agent may reduce the incidence and severity of hemodynamic instability during EVT. Therefore, it is of significant research value to investigate whether the use of ciprofol for general anesthesia is beneficial in AIS patients undergoing EVT.

研究の種類

介入

入学 (推定)

124

段階

  • フェーズ 4

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Pudong New Area
      • Shanghai、Pudong New Area、中国
        • Shanghai Jiaotong University School of Medicine
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. Age ≥18 years.
  2. Clinical diagnosis of AIS.
  3. CT/MRI-confirmed absence of intracranial hemorrhage.
  4. Eligible for EVT.
  5. NIHSS score ≥2.
  6. ASA physical status I-III.
  7. Signed informed consent.

Exclusion Criteria:

  1. Pre-existing severe neurological deficits (mRS 3-5).
  2. Shock.
  3. Severe cardiac disease.
  4. Contraindications to EVT per AHA guidelines.
  5. Participation in conflicting clinical trials.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:ダブル

武器と介入

参加者グループ / アーム
介入・治療
実験的:Ciprofol
For patients in the ciprofol group, ciprofol will be given as induction of anesthesia (0.2 mg/kg) followed by a continuous infusion (0.8 mg/kg/h) until the end of surgery.
Induction of anesthesia followed by continuous infusion through out surgery. Adjust infusion rate according to BIS (BIS target: 40-60). Adjust vasoactive/hypotensive drugs according to hemodynamics.
アクティブコンパレータ:Propofol
For patients in the propofol group, propofol will be given as induction of anesthesia (1 mg/kg) followed by a continuous infusion (4 mg/kg/h) until the end of surgery.
Induction of anesthesia followed by continuous infusion through out surgery. Adjust infusion rate according to BIS (BIS target: 40-60). Adjust vasoactive/hypotensive drugs according to hemodynamics.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Time-weighted average of SBP under the threshold of 120 mmHg after general anesthesia induction until end of surgery
時間枠:During operation
Time-weighted average (TWA) is a calculation of the depth (in mmHg) of hypotension below the 'threshold' SBP of 120 mmHg*the time spent in hypotension in minutes, this results in an 'area'. To better compare this value between different operations the 'area' can be divided by the total duration of the operation. TWA= (depth hypotension below the 'threshold' in mmHg*time spent in hypotension in minutes)/ total duration operation in minutes.
During operation

二次結果の測定

結果測定
メジャーの説明
時間枠
Cumulative time of SBP <120 mmHg
時間枠:During operation
Represents the cumulative time of SBP under 120 mmHg over the operation time.
During operation
Cumulative time of SBP decreased by 20% from the baseline value
時間枠:During operation
Represents the cumulative time under the baseline SBP over the operation time.
During operation
Norepinephrine equivalent
時間枠:During operation
Norepinephrine, phenylephrine and epinephrine doses along with other vasopressor will be analyzed together during the entire procedure.
During operation
Cognitive function evaluated by 3days 3D-CAM and 90-day T-MoCA
時間枠:3 days and 90 days after operation
Delirium will be assessed in person twice daily during the initial three postoperative days using 3D-CAM or CAM-ICU when patients are intubated. Long-term cognitive function will be assessed by the telephone version of the Montreal Cognitive Assessment (T-MoCA) which is designed for telephone use and is also well-validated and well accepted. MoCA is a well-regarded cognitive assessment tool that has possible scores ranging from 0 to 30 points.
3 days and 90 days after operation
90-day mRS score
時間枠:90 days after operation
The mRS is the preferred disability parameter for clinical trials in stroke. The mRS is an ordinal hierarchical scale incorporating six categories from 0 up to and including 5, and describes the range of disability encountered post stroke. 'Death' is assigned a score of 6.
90 days after operation
24h NIHSS, 24h NIHSS score 0-1 or or improvement more than 8
時間枠:24 hours after operation
Scores on the National Institutes of Health Stroke Scale (NIHSS) range from 0 to 42, with higher scores indicating more severe neurologic deficits. NIHSS score 0-1 or ≥8 points reduction in NIHSS score from baseline indicate neurological function recovery and improvement.
24 hours after operation
24h recanalization status
時間枠:24 hours after operation
Occurrence 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 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).
24 hours after operation
48h infarct volume
時間枠:48 hours after operation
Infarct volume will be assessed with the use of an automated, validated algorithm. Infarct size at 48h will be compared with imaging examination results at baseline.
48 hours after operation
90-day mortality
時間枠:90 days after operation
The proportion of all patients who died in each group.
90 days after operation
Safety Assessments
時間枠:90 days after operation

Safety assessments will be conducted during the screening period, throughout the study, and after study completion. Investigators may perform additional safety evaluations during the treatment period as clinically indicated. Participants who discontinue the study early should undergo an end-of-study visit and safety assessment prior to withdrawal. During the trial, the following safety variables will be recorded regularly.

Monitor frequency of adverse events, alterations in clinical safety parameters (changes in physical examination, oxygen saturation, systolic/diastolic blood pressure, pulse) and laboratory tests (Complete blood count, blood chemistry tests, coagulation function).

90 days after operation

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研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年7月1日

一次修了 (推定)

2028年1月31日

研究の完了 (推定)

2028年5月31日

試験登録日

最初に提出

2026年7月6日

QC基準を満たした最初の提出物

2026年7月6日

最初の投稿 (実際)

2026年7月10日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月10日

QC基準を満たした最後の更新が送信されました

2026年7月6日

最終確認日

2026年7月1日

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