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NCT Number: NCT04117672

Antisecretory Factor In Severe Traumatic Brain Injury

This study evaluates the addition of Salovum, an egg yolk powder enriched for antisecretory factor, to standard care of participants with severe traumatic brain injury. Half of the participants will be administered Salovum while the other half will be given a placebo egg yolk powder, not enriched for antisecretory factor. Intracranial pressure (ICP), partial brain oxygen pressure (PtbO2), microdialysis of metabolites and inflammatory mediators and trauma intensity level (TIL) will be assessed in all patients.

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Key information

Age range

10 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Skane University Hopsital

Lund, 22185, Sweden

Location status: Recruiting

Location contact

David Cederberg, MD

CONTACT

[email protected]

About this study

Cerebral edema accounts for an essential part of the morbidity and mortality in severe traumatic brain injury but can also arise in other cerebral pathologies such as infectious and ischemic conditions such e.g. stroke and meningitis. Cerebral edema can lead to an elevated intracranial pressure (ICP) with impact on both perfusion and diffusion in the brain.

AF (antisecretory factor) is a 41 kilodalton endogenous and essential protein with proposed antisecretory and anti-inflammatory effects. AF is homologous to S5A and Rpn10 proteins which are parts of the 26S proteasome subunit. AF also shows close homology to angiocidin a protein with reported anti-proliferative and anti-angiogenic properties. The AF protein is cleaved into several active peptides, one of which has been synthesized within a 16 amino acid peptide (AF-16) that has been used in animal experimental studies. Salovum® is a product based on the egg yolk powder B221®, and contains high levels of AF. Salovum® is classified as a food for special medical purposes (FSMP) by the European Food Safety Agency.

AF has shown clinical effects in Mb Ménière, mastitis and meningitis. Experimentally AF-16 and AF have been shown to reduce intracranial pressure and improve outcome in models of traumatic brain injury (TBI) and herpes encephalitis. Preliminary results show reduction of ICP and improved outcome in human traumatic brain injury. A randomized, prospective, double-blinded phase 2-3 in participants with severe traumatic head injury is ongoing at Tygerberg University Hospital, Cape Town, South Africa (ClinicalTrials.gov identification number: NCT03339505).

The antisecretory factor is an endogenous protein and no antibody formation has been demonstrated in human administration. Although Salovum® has been given to hundreds of patients, no side effects have been recorded. Egg yolk allergy is a contraindication but no cases of triggered allergy have been reported.

The mechanisms underlying the effects of antisecretory factor on cerebral edema are not clarified. Immune modulation through effects on myeloid cells, proteasome modulation and effects on ion pumps have been proposed.

The present study intends to clarify mechanisms behind the proposed effect of antisecretory factor in cerebral edema In the present study participants with severe traumatic brain injury as defined in inclusion and exclusion criteria will be randomised to either treatment with Salovum or placebo egg powder during 5 days after enrolment. Randomisation will be performed in blocks and randomisation envelopes will be used with the number inside the envelope. Salovum and normal egg powder will be suspended with tap water and administered through the gastric feeding tube. All participants will receive standard care for severe TBI according to the treatment algorithm at the Neuro Intensive Care Unit (NICU), Department of Neurosurgery, Skåne University Hospital, Lund, Sweden. The algorithm prescribes invasive monitoring of ICP, PtbO2 and metabolites (cerebral microdialysis). As this algorithm includes stepwise co-interventions in order to control ICP and cerebral perfusion pressure (CPP) the TIL score will be used to compensate for the bias of increased co-interventions in either arm. At follow up patients will be assessed for mortality and Glasgow Outcome Scale-Extended (GOSE)

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Severe traumatic brain injury, Glasgow Outcome Scale (GCS) <9 at admission to NICU.

Clinical indication for insertion of intracranial pressure monitor, intracerebral oxygen pressure monitor and microdialysis catheter.

Consultation with relatives or consent from guardians.

Exclusion criteria

Known egg yolk allergy.

Unilateral or bilateral fixed and dilated pupil after initial operative intervention.

Treatment and study plan

Salovum

Dietary Supplement

Active egg yolk powder

Other names: Antisecretory factor

Placebo egg yolk powder

Dietary Supplement

Normal egg yolk powder

Primary outcomes

  1. ICP mean

    Time frame: During intervention, 5 days

    Measured by an intracranial pressure sensor

Secondary outcomes

  1. Concentration of inflammatory cytokines

    Time frame: During intervention, 5 days

    Interleukin-6 (Il-6), interleukin-8 (IL-8) and monocyte chemotactic protein (MCP-1) assessed from microdialysate and plasma by multiplex analysis

Other outcomes

  1. Mortality

    Time frame: At 30 days and 12 months

    Mortality due to traumatic brain injury

  2. Morbidity

    Time frame: At 6 and 12 months

    Assessed by Glagow Outcome Scale-Extended (GOSE). Minimum 1 (full recovery). MAXIMUM 8 (DEAD)

  3. Intracerebral oxygen partial pressure

    Time frame: During intervention, 5 days

    Measured by an intracranial oxygen sensor

  4. Intracerebral oxygen partial pressure

    Time frame: Change from baseline during intervention, up to 6 days

    Lactate/pyruvate ratio assessed by online microdialysis

  5. Treatment intensity level

    Time frame: During intervention, 5 days

    Treatment intensity level (TIL) scale. Minimum 0 (no intervention to control intracranial pressure (ICP)), maximum 38 points (maximum efforts to control ICP)

  6. Treatment intensity level

    Time frame: Change from baseline during intervention, up to 6 days

    Treatment intensity level (TIL) scale. Minimum 0 (no intervention to control intracranial pressure (ICP)), maximum 38 points (maximum efforts to control ICP)

  7. Rate of cerebral metabolism

    Time frame: During intervention, 5 days

    Lactate/pyruvate ratio assessed by online microdialysis

  8. Rate of cerebral metabolism

    Time frame: Change from baseline during intervention, up to 6 days

    Lactate/pyruvate ratio assessed by online microdialysis

  9. Concentration of brain damage markers

    Time frame: During intervention, 5 days

    Glial fibrillary acidic protein (GFAP) and neuron-specific enolase (NSE) assessed from microdialysate and plasma

  10. Concentration of brain damage markers

    Time frame: Change from baseline during intervention, up to 6 days

    Glial fibrillary acidic protein (GFAP) and neuron-specific enolase (NSE) assessed from microdialysate and plasma

  11. ICP area under curve

    Time frame: During intervention, 5 days

    Measured by an intracranial pressure sensor

  12. ICP area under curve

    Time frame: Change from baseline during intervention, up to 6 days

    Measured by an intracranial pressure sensor

  13. ICP mean

    Time frame: Change from baseline during intervention, up to 6 days

    Measured by an intracranial pressure sensor

  14. Concentration of inflammatory cytokines

    Time frame: Change from baseline during intervention, up to 6 days

    Interleukin-6 (Il-6), interleukin-8 (IL-8) and monocyte chemotactic protein (MCP-1) assessed from microdialysate and plasma by multiplex analysis

Study contacts

Contact information is provided by the study sponsor or research team.

David Cederberg, MD

CONTACT

[email protected]

+4646177655

Peter Siesjö, MD, PhD

CONTACT

[email protected]

+4646171274

Sponsors and collaborators

Lead sponsor

Peter Siesjö

Other

Collaborators

  • Lantmannen Medical AB
  • Skane University Hospital

Registry information

Official study title

Evaluation of Antisecretory Factor in Treatment of Severe Traumatic Brain Injury With Multimodal Monitoring

Acronym: AFISTBI

Important dates

Study start
2020
Primary completion
2026
Study completion
2027
First posted
Oct 7, 2019
Registry last updated
Jan 21, 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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