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NCT Number: NCT07365475

Efficacy and Safety of Intra-Arterial Albumin as Adjunct to Mechanical Thrombectomy in Acute Ischemic Stroke

Stroke remains a predominant global public health challenge, ranking as the third leading cause of death and the fourth leading contributor to disability-adjusted life years (DALYs). According to the Global Burden of Disease Study 2021, there are approximately 93.8 million prevalent stroke cases and 11.9 million new cases worldwide. China bears one of the heaviest burdens, with over 2 million new cases annually. Acute ischemic stroke (AIS), caused by acute cerebrovascular occlusion, accounts for 80% of all strokes. Approximately 30% of AIS cases result from large vessel occlusion (LVO), which typically carries a poor prognosis due to the extensive area of infarction . Research indicates that early recanalization significantly improves clinical outcomes. Currently, intravenous thrombolysis (IVT) and mechanical thrombectomy (MT) are the standard treatments for achieving recanalization . For LVO-related AIS, MT has become the preferred clinical approach due to its extended therapeutic window and superior recanalization rates . However, despite successful recanalization in over 70% of patients, nearly 50% fail to achieve functional independence at 90 days, and mortality remains above 15% . Therefore, enhancing long-term functional outcomes in post-MT patients is a critical unmet clinical need. Human albumin is the most abundant protein in plasma. Beyond maintaining colloid osmotic pressure, it also possesses multiple biological effects, including anti-inflammatory, anti-platelet aggregation, antioxidant, and endothelial protective properties. We conducted a Phase I clinical trial (AMASS-1) for patients post-mechanical thrombectomy, administering human albumin via the internal carotid artery. The results showed that intra-arterial infusion of 20% human albumin at a dose of 0.60 g/kg was safe, with no significant differences in serious adverse reactions such as mortality [Albumin group (6.7%) vs Control group (6.7%), P > 0.05] and symptomatic intracranial hemorrhage [Albumin group (6.7%) vs Control group (13.3%), P > 0.05] compared to the control group. In summary, albumin adjunctive therapy demonstrates good safety and potential neuroprotective effects in patients after mechanical thrombectomy. To further systematically evaluate its efficacy and safety, we plan to conduct a Phase II clinical trial of mechanical thrombectomy combined with intra-arterial albumin infusion for acute ischemic stroke. This is a multicenter, prospective, open-label, endpoint-blinded, randomized controlled trial designed to evaluate the efficacy and safety of intra-arterial infusion of 20% human serum albumin combined with mechanical thrombectomy versus mechanical thrombectomy alone in patients with acute ischemic stroke due to anterior circulation large vessel occlusion who have achieved recanalization after mechanical thrombectomy. A total of 306 patients are planned to be enrolled and randomly assigned in a 1:1 ratio using a dynamic minimization method to two groups: the Albumin Group (0.6 g/kg 20% human serum albumin plus Mechanical Thrombectomy) and the Control Group (Mechanical Thrombectomy alone). The primary efficacy objective of this study is to evaluate whether immediate intra-arterial infusion of 20% human albumin (0.6 g/kg) via the internal carotid artery following successful recanalization (eTICI ≥2b) improves clinical outcomes in patients with acute anterior circulation large vessel occlusion stroke, compared with mechanical thrombectomy alone. The study also aims to evaluate the safety and feasibility of immediate intra-arterial infusion of 20% human albumin (0.6 g/kg) via the internal carotid artery in patients with acute anterior circulation large vessel occlusion stroke who have achieved successful recanalization (eTICI ≥2b) following standard mechanical thrombectomy.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years
  • Acute anterior circulation large vessel occlusion (including ICA/MCA-M1 tandem occlusion or isolated MCA-M1 occlusion) confirmed by CTA, MRA, or DSA, with successful recanalization (eTICI score ≥2b) confirmed by the final intraoperative DSA following mechanical thrombectomy
  • Baseline NIHSS scores ≥ 6
  • Non-contrast CT ASPECTS ≥6
  • Time from stroke onset (or last known well) to arterial puncture within 24 hours
  • Pre-stroke functional independence, defined as a modified Rankin Scale (mRS) score <2
  • Written informed consent obtained from the patient or a legally authorized representative

Exclusion criteria

  • Intracranial hemorrhage confirmed by cranial CT or MRI
  • Midline shift with significant mass effect on cranial CT or MRI
  • Isolated internal carotid artery (ICA) occlusion
  • History of heart failure or severe cardiovascular disease, including but not limited to pulmonary hypertension or pericardial effusion
  • Hemodynamically unstable arrhythmia (based on patient self-report or detected prior to infusion)
  • Symptoms or electrocardiographic evidence of acute myocardial infarction upon admission
  • Acute or chronic renal failure (serum creatinine >2.0 mg/dL
  • Severe anemia (hematocrit <32%
  • Known hypersensitivity to albumin or blood products
  • Pregnancy
  • Persistent hypertension (blood pressure ≥180/100mmHg) prior to albumin infusion
  • Current participation in other clinical trials
  • Life expectancy of less than 3 months
  • Concomitant severe pulmonary disease, such as chronic obstructive pulmonary disease, pulmonary fibrosis, pleural effusion, or acute respiratory distress syndrome
  • Any other condition that, in the opinion of the investigator, renders the patient unsuitable for participation in the study

Treatment and study plan

20% human serum albumin

Drug

20% human albumin solution at a dose of 0.60g/kg will be administered as a constant-rate infusion into the proximal internal carotid artery over 20 minutes.

Primary outcomes

  1. Distribution of mRS scores at 90 (±14) days post-randomization

    Time frame: at 90 (±14) days post-randomization

    Distribution of mRS scores

Secondary outcomes

  1. Proportion of subjects with a favorable outcome at 90 (±14) days post-randomization (defined as mRS 0-2);

    Time frame: at 90 (±14) days post-randomization

    Proportion of subjects with a favorable outcome, defined as mRS 0-2

  2. Proportion of subjects with functional independence at 90 (±14) days post-randomization (defined as mRS 0-1)

    Time frame: at 90 (±14) days post-randomization

    Proportion of subjects with functional independence, defined as mRS 0-1

  3. Infarct volume at 24 (±6) hours post-randomization (measured via MRI-DWI)

    Time frame: at 24 (±6) hours post-randomization

    Infarct volume, measured via MRI-DWI

  4. Infarct volume growth from baseline to 24 (±6) hours post-randomization

    Time frame: from baseline to 24 (±6) hours post-randomization

    Infarct volume growth

  5. Recanalization rate at 24 (±6) hours post-randomization

    Time frame: at 24 (±6) hours post-randomization

    Recanalization rate

  6. NIHSS score at 24 (±6) hours post-randomization

    Time frame: at 24 (±6) hours post-randomization

    NIHSS score

  7. NIHSS score at 7 (±1) days or at discharge, whichever occurs first

    Time frame: at 7 (±1) days or at discharge, whichever occurs first

    NIHSS score

  8. EQ-5D-5L score at 90 (±14) days post-randomization

    Time frame: at 90 (±14) days post-randomization

    EQ-5D-5L score

  9. Proportion of subjects with a Barthel Index (BI) ≥95 at 90 (±14) days post-randomization

    Time frame: at 90 (±14) days post-randomization

    Proportion of subjects with a Barthel Index (BI)

  10. Distribution of mRS scores at 180 (±30) days and 1 year (±30 days) post-randomization

    Time frame: at 180 (±30) days and 1 year (±30 days) post-randomization

    Distribution of mRS scores

  11. Proportion of subjects with a favorable outcome (mRS 0-2) at 180 (±30) days and 1 year (±30 days) post-randomization

    Time frame: at 180 (±30) days and 1 year (±30 days) post-randomization

    Proportion of subjects with a favorable outcome (mRS 0-2)

  12. EQ-5D-5L score at 180 (±30) days and 1 year (±30 days) post-randomization

    Time frame: at 180 (±30) days and 1 year (±30 days) post-randomization

    EQ-5D-5L score

  13. Proportion of subjects with a Barthel Index (BI) ≥95 at 180 (±30) days and 1 year (±30 days) post-randomization

    Time frame: at 180 (±30) days and 1 year (±30 days) post-randomization

    Proportion of subjects with a Barthel Index (BI) ≥95

  14. All-cause mortality within 90 (±14) days post-randomization

    Time frame: within 90 (±14) days post-randomization

    All-cause mortality

  15. Symptomatic intracranial hemorrhage (sICH) at 24 (±6) hours post-randomization (according to ECASS III criteria)

    Time frame: at 24 (±6) hours post-randomization

    Symptomatic intracranial hemorrhage (sICH) ,according to ECASS III criteria

  16. Serious adverse events (SAEs) within 90 (±14) days post-randomization

    Time frame: within 90 (±14) days post-randomization

    SAEs

  17. Adverse events (AEs) within 90 (±14) days post-randomization

    Time frame: within 90 (±14) days post-randomization

    AEs

  18. Early neurological deterioration (END), defined as an increase in NIHSS score of ≥4 points from baseline at 24 hours post-randomization

    Time frame: from baseline at 24 hours post-randomization

    END, defined as an increase in NIHSS score of ≥4 points from baseline at 24 hours post-randomization

  19. Proportion of subjects with severe disability at 90 (±14) days post-randomization (defined as mRS 4-6)

    Time frame: at 90 (±14) days post-randomization

    Proportion of subjects with severe disability , defined as mRS 4-6

  20. Albumin-related adverse events within 90 (±14) days post-randomization

    Time frame: within 90 (±14) days post-randomization

    Albumin-related adverse events

  21. SAEs and AEs within 180 (±30) days post-randomization

    Time frame: within 180 (±30) days post-randomization

    SAEs and AEs

  22. SAEs and AEs within 1 year (±30 days) post-randomization

    Time frame: within 1 year (±30 days) post-randomization

    SAEs and AEs

Other outcomes

  1. Levels of inflammatory cytokines (IL-1β, TNF-α, IL-6, IL-10) in the blood at 24 (±6) hours post-randomization

    Time frame: at 24 (±6) hours post-randomization

    Levels of inflammatory cytokines (IL-1β, TNF-α, IL-6, IL-10) in the blood

  2. Serum albumin and B-type natriuretic peptide (BNP) levels at 24 (±6) hours post-randomization

    Time frame: at 24 (±6) hours post-randomization

    Serum albumin and B-type natriuretic peptide (BNP) levels

  3. Levels of inflammatory cytokines (IL-1β, TNF-α, IL-6, IL-10) in the blood at 7 (±1) days post-randomization or at discharge (whichever occurs first)

    Time frame: at 7 (±1) days post-randomization or at discharge (whichever occurs first)

    Levels of inflammatory cytokines (IL-1β, TNF-α, IL-6, IL-10) in the blood

  4. Serum albumin and BNP levels at 7 (±1) days post-randomization or at dis charge (whichever occurs first)

    Time frame: at 7 (±1) days post-randomization or at dis charge (whichever occurs first)

    Serum albumin and BNP levels

  5. Net water uptake (NWU) at 24 (±6) hours post-randomization

    Time frame: at 24 (±6) hours post-randomization

    Net water uptake (NWU)

  6. Progression of net water uptake from baseline to 24 (±6) hours post-randomization

    Time frame: from baseline to 24 (±6) hours post-randomization

    Progression of net water uptake

  7. Cerebrospinal fluid (CSF) volume at 24 (±6) hours post-randomization

    Time frame: at 24 (±6) hours post-randomization

    Cerebrospinal fluid (CSF) volume

  8. Change in cerebrospinal fluid volume from baseline to 24 (±6) hours post-randomization

    Time frame: from baseline to 24 (±6) hours post-randomization

    Change in cerebrospinal fluid volume

  9. Analysis of the Index for Connectivity via Perivascular Spaces (ALPS index) at 24 (±6) hours post-randomization

    Time frame: at 24 (±6) hours post-randomization

    Analysis of the Index for Connectivity via Perivascular Spaces (ALPS index)

Sponsors and collaborators

Lead sponsor

Tianjin Huanhu Hospital

Other

Registry information

Official study title

Efficacy and Safety of Intra-Arterial Albumin as Adjunct to Mechanical Thrombectomy in Acute Ischemic Stroke: A Multicenter, Prospective, Open-Label, Endpoint-Blinded, Randomized Controlled Clinical Trial (AMASS2)

Acronym: AMASS2

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Jan 26, 2026
Registry last updated
Jan 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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