Investigational Medical Device · Perioperative Airway Safety

Rethinking aspiration prophylaxis.

Aspirvent is a first-in-class alginate-based intragastric barrier device, forming a coherent gel raft on the gastric surface to physically prevent pulmonary aspiration during anesthesia induction and sedation.

1 in 8 Adults currently taking a GLP-1 drug KFF, 2025
>2 in 3 Perioperative aspiration patients who died or suffered permanent severe injury ASA Closed Claims, Anesthesiology 2021
~30% Mortality risk of aspiration pneumonia in surgical patients Studer et al., Int J Surg 2016
0 FDA-cleared mechanical barriers FDA 510(k) & De Novo database, April 2026

Clinical Urgency

A silent crisis in perioperative airway safety.

GLP-1 receptor agonists can delay gastric emptying enough that patients may still have residual gastric contents despite standard pre-operative fasting. The vulnerable moment is practical and specific: immediately before and during induction of general anesthesia, when consciousness and airway reflexes are impaired.

GLP-1 first

Aspira is prioritizing patients on GLP-1 therapy before expanding into broader pre-operative gastric-content protection.

High RGC

GLP-1 RAs delay gastric emptying, resulting in elevated residual gastric contents before anesthesia. Pai et al., Anesth Analg 2026

57%

Most common complication reported by clinicians who witnessed perioperative complications in GLP-1 patients. Brennan et al., Turk J Anaesthesiol Reanim 2025

$4.2B

Annual US cost burden of aspiration pneumonia, pneumonitis, and related ICU admissions. HCUP National Inpatient Sample, 2022

None

FDA-cleared intragastric mechanical barrier devices for aspiration prophylaxis on the market today. FDA 510(k) & De Novo database, April 2026

Problem · Primary Target Population

GLP-1 patients first, then broader pre-operative patients who need gastric-content aspiration protection.

Aspirvent is positioned as a practical pre-induction adjunct for patients whose gastric emptying is unpredictable. The initial focus is GLP-1 therapy, where delayed gastric emptying is directly changing anesthesia workflow and cancellation risk.

No evidence RSI reduces aspiration risk (Neilipovitz & Crosby, Can J Anaesth 2007)
1 in 8 adults currently taking a GLP-1 drug
0 FDA-cleared intragastric barrier devices
GLP-1 Risk Landscape
Relative perioperative signal High Mid Low 40M+ 2-4x 0 Rx volume Risk Barriers
GLP-1 prescriptions have altered the perioperative aspiration-risk landscape, with no device-based aspiration protection available.

Aspirvent Mechanism

Gastric physics, engineered.

When swallowed, Aspirvent's alginate-based matrix expands to create a pressure-resistant seal at the gastroesophageal junction, delivering measurable, benchmarked protection against regurgitation.

Aspirvent raft mechanism Diagram showing swallowed liquid entering the stomach, forming a floating raft seal at the gastroesophageal junction above gastric contents. floating raft seal gastric contents GEJ
Liquid dose HCl activation CO2 buoyancy + Ca2+ crosslinking Raft caps gastric contents
01

Ingest Liquid

An orally administered liquid is taken before the vulnerable peri-induction window, designed to fit into pre-operative workflows before anesthesia induction.

02

Acid Triggers Raft Formation

Gastric HCl protonates alginate; bicarbonate generates CO2 microbubbles; calcium crosslinks the alginate network in acidic gastric conditions.

03

Seal Resists Pressure

The buoyant raft is designed to seal at the gastroesophageal junction and resist upward movement during laryngoscopy and induction.

04

Natural Clearance

After the peri-induction risk window, the alginate raft is intended to clear through normal gastric processes without a systemic pharmacologic footprint.

Scientific Foundation

Built on decades of alginate science.

Chemistry

Alginate gel-raft technology

Sodium alginate cross-links with divalent calcium ions in the gastric environment to form a coherent viscoelastic gel raft.

IP Status

PCT patent application filed

International patent application filed March 2026 covering device composition, method of use, and novel formulation embodiments.

Development Plan

GMP-capable development partner

CMC development and GMP-grade formulation manufacturing partnership in place to support regulatory submissions and the first-in-human imaging study.

Scientific Foundation

Peer-reviewed science

Aspira is translating bench formulation work and perioperative aspiration-prevention scholarship into a focused medical-device development program.

Focal Point

Anesthesiology · Focal Point Article

[Title withheld pending publication]

Olsen K, et al. — Revise & Resubmit under review

Revise & Resubmit
Original

Anesthesia & Analgesia · Original Article

A novel method to reduce aspiration risk in anesthesia and critical care settings using alginate gel formulation

Jones A, Olsen K, Pepe A — Accepted April 2026

Accepted

Development Roadmap

Aspirvent roadmap.

Staged development designed to reach first-in-human data with minimal cash outlay through equity-based partnerships.

Aspirvent

Alginate gel raft · Oral solution · Investigational medical device

Active development

Active Development
Primary indication
GLP-1 patient perioperative aspiration prophylaxis
Study design
First-in-human fluoroscopy & ultrasound imaging study
Regulatory
Q-Sub Pre-Submission → IDE → First-in-Human → De Novo
  1. IP & LicenseFoundation
  2. CMC / Q-SubActive
  3. IDENext
  4. First-in-HumanImaging
  5. De NovoRegulatory path

Team

The team behind Aspira.

Leadership and advisors advancing Aspira's investigational medical device program.

Kevin Olsen, MD
Kevin Olsen, MD
Founder & CEO

Triple board-certified anesthesiologist in Anesthesiology, Critical Care, and Neurocritical Care. Author of 17 peer-reviewed publications.

Anesthesiology Critical Care Neurocritical Care
-
To be announced
Lead Chemist · Co-Inventor

Expert in alginate polymer chemistry and biomaterial formulation. Co-inventor on the PCT patent covering Aspirvent's core composition, gel-raft mechanism, and novel formulation embodiments.

Polymer Chemistry Biomaterials GMP Formulation
-
To be announced
Scientific Advisor · Co-Inventor

Anesthesiologist with expertise in perioperative patient safety and oncologic anesthesia. Co-inventor and clinical collaborator for the first-in-human fluoroscopy imaging study design.

Anesthesiology Clinical Research Patient Safety
Building the team that protects every airway.

Interested in joining Aspira's scientific, clinical, or regulatory advisory bench?

Get in touch