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Exploring the Combination of Intracalvariosseous and Intravenous Antibiotics for Moderate to Severe Bacterial Meningitis (SPARK)

2026年9月13日 更新者:yilong Wang

Feasibility, Safety, and Preliminary Efficacy of Combined Intracalvariosseous and Intravenous Antibiotic Infusion for Moderate to Severe Bacterial Meningitis

Multiple preclinical and clinical studies, including the investigators' published work and the ongoing SOLUTION series trials, have consistently demonstrated that intracalvariosseous (ICO) injection can markedly increase drug exposure in the central nervous system with an acceptable safety profile. This is a multicenter, prospective, single-arm, open-label, exploratory clinical study designed to evaluate the feasibility, safety and preliminary efficacy of antibiotic delivery via the ICO route combined with standard intravenous therapy in patients with moderate-to-severe bacterial meningitis who have shown an inadequate response to standard antibiotic treatment.

調査の概要

詳細な説明

Bacterial meningitis remains a major cause of death and long-term neurological disability despite advances in antimicrobial therapy, vaccination and critical care. Moderate-to-severe disease, particularly healthcare-associated ventriculitis/meningitis and infections caused by multidrug-resistant (MDR) pathogens, continues to pose substantial therapeutic challenges. Intravenous antibiotic therapy alone often fails to achieve sufficiently rapid and sustained therapeutic drug concentrations in cerebrospinal fluid (CSF) and at the meningeal surface due to the blood-brain barrier. Although intrathecal and intraventricular administration can increase local drug concentrations, these approaches carry high complication risks and have limited diffusion in the subarachnoid space.

Anatomical and physiological studies have demonstrated direct communication pathways between calvarial bone marrow, dura mater, CSF spaces and the glymphatic system, providing a biological rationale for intracalvariosseous (ICO) injection as a regional drug delivery route to the central nervous system. Preclinical and clinical evidence, including the investigators' published work and the ongoing SOLUTION series clinical trials, confirms that ICO delivery can enhance local CNS drug exposure without disrupting the blood-brain barrier, with a manageable safety profile. In addition, the investigators' exploratory animal study of vancomycin delivered via ICO in a bacterial meningitis model further demonstrated improved anti-infective efficacy at reduced systemic doses.

This trial is a multicenter, prospective, single-arm, open-label, exploratory clinical study. A total of 9 eligible patients will be enrolled across 3+ medical centers led by Beijing Tiantan Hospital, Capital Medical University.

Eligible participants are adults aged 18-75 years with moderate-to-severe bacterial meningitis who show no improvement or clinical deterioration after a course of empiric or targeted intravenous antibiotic therapy, and for whom treatment with polymyxin B, tigecycline or vancomycin is clinically indicated.

All enrolled participants will receive guideline-concordant standard supportive care (including intracranial pressure management, seizure control, organ support and symptomatic treatment) plus optimized intravenous antibiotic therapy. In addition, all participants will undergo bilateral parietal burr hole placement of cranial bolt delivery devices, followed by continuous infusion of the selected antibiotic via the calvarial bone marrow route for 7 consecutive days (7×24 hours). The ICO delivery device will be removed after the 7-day infusion course, and the duration of subsequent intravenous antibiotic therapy will be adjusted according to clinical and laboratory response. Rescue intrathecal or intraventricular antibiotic therapy will be initiated if predefined criteria of no improvement are met within the first 3 days of combined treatment.

Study visits are scheduled at:

Baseline (screening and enrollment) Day 1 (ICO device placement and treatment initiation) Days 2-4 (early efficacy assessment) Day 8 Day 15 Month 1 (±3 days) Month 3 (±7 days, telephone follow-up) A Data and Safety Monitoring Board (DSMB) will regularly monitor safety and study conduct throughout the trial. The study has been approved by the Institutional Review Board / Ethics Committee of Beijing Tiantan Hospital, Capital Medical University.

研究の種類

介入

入学 (推定)

9

段階

  • 適用できない

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

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100071
        • Beijing Tiantan Hospital, Beijing

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 18-75 years, gender not limited;
  • 2. Meeting the diagnostic criteria for moderate-to-severe bacterial meningitis:

Meeting the diagnostic criteria for bacterial meningitis (at least item i must be satisfied):

i. Clinical diagnosis: abnormal body temperature (>38 ℃ or <36 ℃), turbid or purulent cerebrospinal fluid (CSF), CSF leukocytosis (>500 × 10⁶/L), CSF glucose/serum glucose ratio < 0.4, CSF protein concentration > 50 mg/dL; ii. Etiological diagnosis: on the basis of item i, positive microbial detection or culture from specimen smears, drainage catheter tips, implants or CSF (excluding contamination and colonization).

Glasgow Coma Scale (GCS) score ≤ 12, or a decrease of ≥ 2 points from the previous assessment; At least one of the following: altered consciousness, seizures, brain parenchymal involvement, mechanical ventilation, or circulatory support.

  • 3. No significant improvement or progressive worsening of the condition after empirical or targeted antibiotic therapy, as confirmed by at least 2 consecutive treatment evaluations, with at least one of the following: No relief or worsening of intracranial infection-related signs and symptoms; No decreasing trend in CSF white blood cell count, or re elevation after an initial decrease; No decreasing trend in CSF protein concentration, or re elevation after an initial decrease; No increasing trend in CSF/serum glucose concentration ratio, or re decrease after an initial increase; Persistently positive CSF bacterial culture, or re positivity after initial negative conversion.
  • 4. Treatment with polymyxin B, tigecycline or vancomycin is clinically indicated for intracranial anti infective therapy, as judged by the investigator.
  • 5. Written informed consent obtained.

Exclusion Criteria:

  • 1. History of allergy to polymyxin B, tigecycline or vancomycin;
  • 2. Unilateral skull craniotomy edge within 30 mm of the parietal eminence, as confirmed by cranial imaging or physical measurement;
  • 3. Severe pulmonary infection / acute respiratory distress syndrome (PaO₂/FiO₂ < 150 mmHg, FiO₂ ≥ 0.6, PEEP ≥ 5 cmH₂O), or mechanical ventilation whose primary cause is not intracranial infection;
  • 4. Primary extracranial focus of infection (e.g., lung, abdomen, urinary tract) requiring vasoactive agents to maintain MAP ≥ 65 mmHg (e.g., norepinephrine ≥ 0.25 μg/kg/min) and lactate > 2 mmol/L after adequate fluid resuscitation, or critical illness whose primary cause is not intracranial infection;
  • 5. Contraindications to intracalvariosseous (ICO) administration: severe skull fracture, poor visualization of the calvarial diploic space, planned decompressive craniectomy, or other conditions that may interfere with ICO drug delivery;
  • 6. Clinical signs of brain herniation: unilateral or bilateral pupillary dilation and fixation; loss of other brainstem reflexes judged by the investigator to be caused by meningitis or brain herniation; or other uncontrollable signs of vital sign instability;
  • 7. Bleeding tendency considered unfavorable for the procedure by the investigator: coagulopathy (e.g., platelet count < 50 × 10⁹/L; prothrombin time [PT] prolongation > 3 seconds), or previously diagnosed hemophilia or other coagulation disorders;
  • 8. Severe hepatic or renal insufficiency: Severe hepatic insufficiency: alanine aminotransferase (ALT) ≥ 3 × upper limit of normal (ULN) or aspartate aminotransferase (AST) ≥ 3 × ULN; Severe renal insufficiency: serum creatinine (CRE) ≥ 1.5 × ULN or estimated glomerular filtration rate (eGFR) < 40 mL/min/1.73 m²;
  • 9. Acute ST segment elevation myocardial infarction and/or decompensated heart failure (New York Heart Association [NYHA] class III or IV) within the past 3 months;
  • 10. Active hepatitis B infection (positive hepatitis B surface antigen and/or serum HBV DNA positive, or serum HBV DNA > 2 × 10⁸ IU/mL);
  • 11. Positive hepatitis C virus antibody or history of positive testing;
  • 12. Positive HIV test or history of positive testing;
  • 13. Pregnant, lactating, or potentially pregnant patients, or patients planning pregnancy;
  • 14. Currently participating in other interventional trials, or having received other investigational drugs within 1 month or 5 drug half lives;
  • 15. Patients deemed unsuitable for the study by the investigator.

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:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Intracalvariosseous injection + Intravenous injection
In patients who fail to respond to the initial intravenous antibiotic regimen, intravenous treatment will be switched to the indicated antibiotic (polymyxin B, tigecycline, or vancomycin). At the same time, bilateral parietal outer-table drill holes will be created, delivery devices will be secured, and the corresponding antibiotic (polymyxin B, tigecycline, or vancomycin) will be continuously infused via the intracalvariosseous route. The combined ICO and intravenous treatment will be administered concurrently for 7 × 24 hours, after which the ICO devices will be removed. The duration of intravenous therapy will then be adjusted according to treatment response, including clinical symptoms, signs, and laboratory findings.
ポリミキシンB(12.5 mg/日)、チゲサイクリン(12.5 mg/日)、およびバンコマイシン(125 mg/日)の持続的頭蓋骨内注入。
ポリミキシンB(100mg/日)、チゲサイクリン(100mg/日)、バンコマイシン(2000mg/日)の静脈内投与。
治療期間全体を通じて関連ガイドラインに基づく標準的な治療と管理

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
Feasibility and safety of cranial burr hole procedure and 7-day continuous intracalvariosseous antibiotic infusion
時間枠:From Day 1 (device placement) to Day 8 (device removal)
Success rate of parietal burr hole placement; proportion of participants who complete 7×24-hour continuous antibiotic infusion via the intracalvariosseous route; incidence of device dislodgement, leakage, occlusion and unplanned infusion interruption.
From Day 1 (device placement) to Day 8 (device removal)
Proportion of participants requiring rescue intrathecal/intraventricular antibiotic therapy within 3 days after intervention initiation
時間枠:Within 3 days after initiation of intracalvariosseous treatment, such as Day 2, 3, 4.

The proportion of participants who meet predefined inadequate response criteria within the first 3 days (such as Day 2, 3, 4) of combined therapy and thus receive rescue intrathecal (IT) or intraventricular (IVT) antibiotics.

Inadequate response is defined as ≥2 of the following 4 items showing no improving trend or deterioration compared with baseline in at least 2 consecutive clinical evaluations:

Intracranial infection-related clinical signs and symptoms Cerebrospinal fluid (CSF) white blood cell count CSF protein concentration CSF/serum glucose concentration ratio

Within 3 days after initiation of intracalvariosseous treatment, such as Day 2, 3, 4.
Overall clinical response rate at Day 8 and Day 15
時間枠:Day 8, Day 15 after intervention initiation

Overall response rate = [(Cure + Improvement) / Total number of evaluable participants] × 100% Cure: CSF white blood cell count, CSF protein concentration, CSF/serum glucose ratio, and CSF bacterial culture are all normal in 2 consecutive tests.

Improvement: All 4 above CSF indicators are normal in at least 1 test. Ineffective: All 4 above CSF indicators remain abnormal in 2 consecutive tests.

Normal reference values for CSF indicators:

White blood cell count: < 100 × 10⁶/L Protein concentration: < 50 mg/dL CSF/serum glucose ratio: > 0.5

Day 8, Day 15 after intervention initiation

二次結果の測定

結果測定
メジャーの説明
時間枠
Cure rate at Day 8 and Day 15
時間枠:Day 8, Day 15 after intervention initiation
Definition: Proportion of participants meeting the "Cure" criteria defined above.
Day 8, Day 15 after intervention initiation
Improvement rate at Day 8 and Day 15
時間枠:Day 8, Day 15 after intervention initiation
Definition: Proportion of participants meeting the "Improvement" criteria defined above.
Day 8, Day 15 after intervention initiation
Cerebrospinal fluid white blood cell count at Days 2-4 and Day 8, Day 15 after intervention initiation
時間枠:Days 2-4 and Day 8, Day 15 after intervention initiation
Cerebrospinal fluid white blood cell count
Days 2-4 and Day 8, Day 15 after intervention initiation
Cerebrospinal fluid protein concentration at Days 2-4 and Day 8, Day 15 after intervention initiation
時間枠:Days 2-4 and Day 8, Day 15 after intervention initiation
Cerebrospinal fluid protein concentration
Days 2-4 and Day 8, Day 15 after intervention initiation
Cerebrospinal fluid-to-serum glucose concentration ratio at Days 2-4 and Day 8, Day 15 after intervention initiation
時間枠:Days 2-4 and Day 8, Day 15 after intervention initiation
Cerebrospinal fluid-to-serum glucose concentration ratio
Days 2-4 and Day 8, Day 15 after intervention initiation
CSF bacterial culture results and pathogen clearance status
時間枠:Days 2-4 and Day 8, Day 15 after intervention initiation
Cerebrospinal fluid bacteriological culture results
Days 2-4 and Day 8, Day 15 after intervention initiation
Glasgow Coma Scale (GCS) score and its change from baseline
時間枠:Days 2-4 and Day 8, Day 15 after intervention initiation
GCS assesses consciousness level via 3 components (eye opening, verbal response, motor response). Total score ranges 3-15; higher scores indicate better neurological status.
Days 2-4 and Day 8, Day 15 after intervention initiation
All-cause mortality within 14 days of intervention initiation
時間枠:Within 14 days of the start of the intervention
All-cause mortality is equal to the ratio of the number of all-cause deaths to the total number of cases within the same treatment group
Within 14 days of the start of the intervention
Mortality due to meningitis within 14 days of intervention initiation
時間枠:Within 14 days of the start of the intervention
Mortality due to meningitis. The diagnostic criteria are the absence of a downward trend in the cerebrospinal fluid leukocyte count, protein concentration, and the ratio of cerebrospinal fluid glucose concentration to serum glucose concentration prior to death.
Within 14 days of the start of the intervention
Antibiotic concentrations in CSF and plasma, and CSF/plasma concentration ratio
時間枠:0.25, 0.5, 1, 2, 4, 8, 12, 24 hours and Days 2-4, Day 8 after intervention initiation.
The ratio of cerebrospinal fluid drug concentration to plasma drug concentration
0.25, 0.5, 1, 2, 4, 8, 12, 24 hours and Days 2-4, Day 8 after intervention initiation.
Bacterial culture results of calvarial bone marrow fluid before and after intracalvariosseous treatment
時間枠:Day 1 (device placement) and Day 8 (device removal)
calvarial bone marrow fluid bacteriological culture results
Day 1 (device placement) and Day 8 (device removal)
Glasgow Outcome Scale (GOS) score at 1 month (±3 days), 3 months (±7 days) after intervention initiation
時間枠:1 month (±3 days), 3 months (±7 days) after intervention initiation
5-point functional scale: 1 = death, 2 = vegetative state, 3 = severe disability, 4 = moderate disability, 5 = good recovery. Higher scores indicate better functional outcome
1 month (±3 days), 3 months (±7 days) after intervention initiation
Cure rate without neurological sequelae at 1 month (±3 days), 3 months (±7 days) after intervention initiation
時間枠:1 month (±3 days), 3 months (±7 days) after intervention initiation
Proportion of participants with normalized CSF indicators and no new meningitis-attributable neurological deficits.
1 month (±3 days), 3 months (±7 days) after intervention initiation
All-cause mortality at 1 month (±3 days), 3 months (±7 days) after intervention initiation
時間枠:1 month (±3 days), 3 months (±7 days) after intervention initiation
All-cause mortality is equal to the ratio of the number of all-cause deaths to the total number of cases within the same treatment group
1 month (±3 days), 3 months (±7 days) after intervention initiation
Meningitis-related mortality at 1 month (±3 days), 3 months (±7 days) after intervention initiation
時間枠:1 month (±3 days), 3 months (±7 days) after intervention initiation
Meningitis-related mortality is equal to the ratio of the number of deaths due to meningitis to the total number of cases within the same treatment group. Meningitis-related mortality. The diagnostic criteria are the absence of a downward trend in the cerebrospinal fluid leukocyte count, protein concentration, and the ratio of cerebrospinal fluid glucose concentration to serum glucose concentration prior to death.
1 month (±3 days), 3 months (±7 days) after intervention initiation
Reinfection with the same microorganism occurred at 1 month (±3 days), 3 months (±7 days) after intervention initiation
時間枠:1 month (±3 days), 3 months (±7 days) after intervention initiation
Reinfection with the same microorganism
1 month (±3 days), 3 months (±7 days) after intervention initiation
Breach of the inner table of the skull during calvarial drilling
時間枠:Day 1 (device placement)
Breach of the inner table of the skull
Day 1 (device placement)
Infection events related to intracalvariosseous injection, such as skin infection or calvarial bone marrow osteomyelitis
時間枠:From Day 1 (device placement) to Day 8 (device removal)
For example, skin infection or calvarial bone marrow osteomyelitis
From Day 1 (device placement) to Day 8 (device removal)
First occurrence of seizures after intervention initiation, including seizures considered to be associated with antibiotic use
時間枠:From Day 1 (device placement) to Day 8 (device removal)
Seizures considered to be associated with antibiotic use
From Day 1 (device placement) to Day 8 (device removal)
Nucleated cell count in calvarial bone marrow fluid before and after intracalvariosseous injection
時間枠:Day 1 (device placement) and Day 8 (device removal)
Nucleated cell count in calvarial bone marrow fluid
Day 1 (device placement) and Day 8 (device removal)
Hepatic or renal dysfunction/failure after intervention initiation
時間枠:From Day 1 (device placement) to Day 8 (device removal)
Definition: Hepatic dysfunction/failure is defined as alanine aminotransferase or aspartate aminotransferase levels greater than 3 times the upper limit of normal. Renal dysfunction/failure is defined as serum creatinine greater than 1.5 times the upper limit of normal or an estimated glomerular filtration rate of <40 mL/min/1.73 m²
From Day 1 (device placement) to Day 8 (device removal)
Incidence of sensorineural hearing loss after intervention initiation
時間枠:From Day 1 (device placement) to Day 8 (device removal)
Based on distortion-product otoacoustic emission + multiple auditory steady-state evoked responses / auditory brainstem response. Definition: Compared with baseline, hearing loss is defined as an increase of ≥20 dB at any single frequency, an increase of ≥10 dB at two adjacent frequencies, or an increase of ≥10 dB in the average threshold across three frequencies.
From Day 1 (device placement) to Day 8 (device removal)
Incidence of red man syndrome after intervention initiation
時間枠:From Day 1 (device placement) to Day 8 (device removal)
Red man syndrome is defined as an infusion-related reaction occurring during or shortly after vancomycin administration, characterized by flushing/erythema and pruritus predominantly involving the face, neck, upper trunk, or upper extremities, with or without rash, and possibly accompanied by chest or back pain and/or hypotension, in the absence of features suggesting IgE-mediated anaphylaxis
From Day 1 (device placement) to Day 8 (device removal)
Incidence of skin hypersensitivity reactions after intervention initiation
時間枠:From Day 1 (device placement) to Day 8 (device removal)
For example, rash and urticaria
From Day 1 (device placement) to Day 8 (device removal)
Incidence of gastrointestinal adverse reactions after intervention initiation
時間枠:From Day 1 (device placement) to Day 8 (device removal)
For example, nausea and vomiting
From Day 1 (device placement) to Day 8 (device removal)
Length of stay in the intensive care unit (ICU) after intervention initiation
時間枠:From date of intervention initiation until first ICU discharge or death, whichever comes first, assessed up to 3 months ± 7 days
Calculate the number of days of ICU stay
From date of intervention initiation until first ICU discharge or death, whichever comes first, assessed up to 3 months ± 7 days
Total length of hospital stay after intervention initiation
時間枠:From date of intervention initiation until hospital discharge or death, whichever comes first, assessed up to 3 months ± 7 days
Calculate the number of days from intervention initiation to discharge
From date of intervention initiation until hospital discharge or death, whichever comes first, assessed up to 3 months ± 7 days
Duration of antibiotic use after intervention initiation
時間枠:From date of intervention initiation until discontinuation of systemic antibiotic therapy or death, whichever comes first, assessed up to 3 months ± 7 days
Calculate the number of days from intervention initiation to the discontinuation of antibiotics
From date of intervention initiation until discontinuation of systemic antibiotic therapy or death, whichever comes first, assessed up to 3 months ± 7 days
ICU costs after intervention initiation
時間枠:From date of intervention initiation until first ICU discharge or death, whichever comes first, assessed up to 3 months ± 7 days
Costs from intervention initiation to ICU discharge
From date of intervention initiation until first ICU discharge or death, whichever comes first, assessed up to 3 months ± 7 days
Total hospitalization costs after intervention initiation
時間枠:From date of intervention initiation until hospital discharge or death, whichever comes first, assessed up to 3 months ± 7 days
Total cost from intervention initiation to discharge
From date of intervention initiation until hospital discharge or death, whichever comes first, assessed up to 3 months ± 7 days

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Yilong Wang, PhD, MD、Beijing Tiantan Hospital

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9月21日

一次修了 (推定)

2027年1月31日

研究の完了 (推定)

2027年3月31日

試験登録日

最初に提出

2026年9月13日

QC基準を満たした最初の提出物

2026年9月13日

最初の投稿 (実際)

2026年9月17日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月17日

QC基準を満たした最後の更新が送信されました

2026年9月13日

最終確認日

2026年9月1日

詳しくは

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個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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