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Enrolling by Invitation

NCT Number: NCT06421532

Stimulating Amyloid Clearance in Cerebral Amyloid Angiopathy

A pre-post study will be conducted to assess whether treatment with LXB, nVNS or a combination of both interventions can enhance the clearance of Aβ in patients with CAA. A total of 60 subjects, 30 with sCAA and 30 with D-CAA, will be randomly assigned to receive LXB, or both interventions. The primary outcome measure will be the morning levels of Aβ40 and Aβ42 in cerebrospinal fluid (CSF) before and after the intervention. The investigators will assess disease progression with (non-)haemorrhagic imaging markers on 7-Tesla Magnetic Resonance Imaging (7-T MRI) as a secondary outcome. Additionally, the activity of the glymphatic system by means of fluid dynamics will be assessed using 7-T MRI.

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Key information

Age range

30 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Leiden University Medical Center (LUMC)

Leiden, 2333ZA, Netherlands

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with D-CAA with a proven amyloid precursor protein (APP) mutation or a history of ≥1 lobar intracerebral haemorrhage (ICH) and a positive family history for D-CAA in ≥1 first degree relative
  • Age ≥30 years old
  • ≤ 2 symptomatic ICH (occurrence of ICH at least > 1 year ago) or presence of ≥ 1 haemorrhagic marker (cortical superficial siderosis, cerebral microbleeds) or non-haemorrhagic marker (white matter hyperintensities, enlarged perivascular spaces).
  • When presymptomatic, patients are aware that they have D-CAA
  • Probable sporadic CAA (sCAA) according to the Modified Boston criteria 2.0
  • Age ≥50 years old
  • ≤ 2 symptomatic ICH (occurrence of ICH at least > 1 year ago)
  • Provisional CAA when the criteria for probable sCAA are not met due to presence of deep haemorrhagic lesions but there are mostly lobar microbleeds (MBs) and cortical superficial siderosis (cSS) present or a ratio of 10 times more lobar MBs than deep MBs without cSS.
  • Age ≥50 years old
  • ≤ 2 symptomatic ICH (occurrence of ICH at least > 1 year ago)
  • Participants able to read and understand the patient information folder and who freely provide written informed consent

Exclusion criteria

  • Modified Rankin Score ≥ 4
  • A life expectancy of less than six months
  • Pregnancy/breast feeding
  • Contraindications for lumbar puncture
  • Unwillingness to refrain from consuming > 1 alcohol unit per day and not later than 8 pm, during the intervention period.

Contraindications for using LXB:

  • Sleep apnea; patients will be screened with respiratory polygraphy before inclusion and screening by questionnaire during intervention with LXB.
  • Restless legs (RLS) needing active treatment with RLS medication.
  • Currently suffering from severe depression and using medication or receiving cognitive therapy.
  • Porphyria
  • Succinic semialdehyde dehydrogenase (SSADH-)deficiency
  • Use of opiates, barbiturates, sedatives (dexmedetomidine, temazepam, oxazepam, midazolam)
  • Use certain medication before inclusion:
  • When benzodiazepine is used: a two nights washout before the intervention (T3) will be started, is needed.
  • When LXB or SXB is used before inclusion: one week washout before inclusion and no use of LXB or SXB during inclusion except for the intervention dose.

Contraindications for lumbar puncture:

  • Compression of the spinal cord
  • Signs and symptoms of increased intracranial pressure
  • Local infections of the skin at the puncture site
  • Coagulopathy or thrombocytopenia (<100)
  • (Use of acetylsalicylic acid, NSAIDs, COX2 inhibitors or prophylactic low-molecular-weight heparin are no contraindications for lumbar puncture.)
  • Participants deemed at risk for brain replacement due to known aqueduct stenosis, Arnold chiari malformations.
  • Participants with a lumbo-sacral neural tube defect or who have a ventriculo-atrial or ventriculo-peritoneal drain.

Contraindications for nVNS:

  • An active implantable medical device such as a pacemaker, deep brain stimulator, or any implanted electronic device.
  • A recent (< 1 month) brain infarction or transient ischemic attack due to a symptomatic stenosis or dissection of the carotid artery (in these patients the other side will be stimulated unless a significant stenosis or dissection on the other side is present as well).
  • If someone knows to have a structural abnormality e.g. lymphadenopathy, previous surgery or abnormal anatomy (in these patients the other side will be stimulated)
  • Metal cervical spine hardware or metallic implant near the stimulation site
  • Cervical vagotomy (in these patients the other side will be stimulated)

Contraindications for 7 Tesla MRI as determined by the 7 Tesla safety committee. Examples of possible contra-indications are:

  • Claustrophobia
  • Pacemakers and defibrillators
  • Nerve stimulators
  • Intracranial clips
  • Intraorbital or intraocular metallic fragments
  • Cochlear implants
  • Ferromagnetic implants
  • Hydrocephalus pump
  • Intra-uterine device
  • Permanent make-up
  • Tattoos above the shoulders

Specific contraindications for checkerboard functional Magnetic Resonance Imaging (fMRI):

  • Seizure within prior year
  • Photosensitive epilepsy
  • Non-correctable visual impairment

Treatment and study plan

Xywav

Drug

Daily before bedtime for 3 months

gammaCore Sapphire

Device

Twice daily for 3 months

Primary outcomes

  1. Morning amyloid-beta 40 and 42 levels in cerebrospinal fluid

    Time frame: 3 months

    Difference between before and after intervention

Secondary outcomes

  1. Disease progression with (non-)haemorrhagic imaging markers on 7-T MRI

    Time frame: 2x 3 months

    Macrobleeds

  2. Disease progression with (non-)haemorrhagic imaging markers on 7-T MRI

    Time frame: 2x 3 months

    Cerebral microbleeds

  3. Disease progression with (non-)haemorrhagic imaging markers on 7-T MRI

    Time frame: 2x 3 months

    Cortical superficial siderosis

  4. Disease progression with (non-)haemorrhagic imaging markers on 7-T MRI

    Time frame: 2x 3 months

    Convexity subarachnoid haemorrhage

  5. Disease progression with (non-)haemorrhagic imaging markers on 7-T MRI

    Time frame: 2x 3 months

    Periventricular and deep white matter hyperintensity volume

  6. Disease progression with (non-)haemorrhagic imaging markers on 7-T MRI

    Time frame: 2x 3 months

    Cerebrovascular reactivity

  7. Disease progression with (non-)haemorrhagic imaging markers on 7-T MRI

    Time frame: 2x 3 months

    Interaction between CSF-mobility at the 4th ventricle and brain vasomotion

  8. Disease progression with (non-)haemorrhagic imaging markers on 7-T MRI

    Time frame: 2x 3 months

    Total CAA-related cerebral small vessel disease (CAA-CSVD) score

  9. Activity of the glymphatic system by means of fluid dynamics on 7-T MRI

    Time frame: 2x 3 months

    CSF-mobility (in mm2/s)

  10. Activity of the glymphatic system by means of fluid dynamics on 7-T MRI

    Time frame: 2x 3 months

    Principal orientation of CSF-mobility

  11. Activity of the glymphatic system by means of fluid dynamics on 7-T MRI

    Time frame: 2x 3 months

    Fractional anisotropy

  12. Other liquid biomarkers

    Time frame: 3 months

    Difference in Aβ-levels 40 and 42 in CSF comparing the three intervention groups and the BATMAN placebo control group.

  13. Other liquid biomarkers

    Time frame: 3 months

    Levels of amyloid-beta 38, 43, t-tau and p-tau181 in CSF

  14. Other liquid biomarkers

    Time frame: 3 months

    Levels of amyloid-beta 40 and 42 in serum

  15. Questionnaires

    Time frame: 2x 3 months

    Cognitive status using the Montreal Cognitive Assessment (MoCA)

  16. Questionnaires

    Time frame: 2x 3 months

    Symptoms of depression and anxiety using the Hospital Anxiety and Depression Scale (HADS)

  17. Questionnaires

    Time frame: 2x 3 months

    Quality of life using the 36-item Short Form healthy survey (SF-36)

  18. Questionnaires

    Time frame: 2x 3 months

    Quality of sleep using the Pittsburgh Sleep Quality Index (PSQI)

  19. Questionnaires

    Time frame: 2x 3 months

    Severity of insomnia using the Insomnia Severity Index (ISI)

  20. Intervention monitoring

    Time frame: 3 months

    Compliance, side effects and tolerability of nVNS and LXB

  21. Intervention monitoring

    Time frame: 3 months

    The number of participants developing sleep apnoea during intervention

Sponsors and collaborators

Lead sponsor

Leiden University Medical Center

Other

Collaborators

  • The Dutch Brain Foundation

Registry information

Official study title

A Partial Randomised Clinical Trial Investigating Stimulation of the Glymphatic System by Either Deepening Sleep With Lower-sodium Oxybate or Inhibiting Cortical Spreading Depressions With Non-invasive Vagus Nerve Stimulation, or Both, in Patients With Cerebral Amyloid Angiopathy (CAA)

Acronym: Clear-Brain

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
May 20, 2024
Registry last updated
Feb 24, 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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