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A New and Innovative Method for CO2 Removal in Anesthetic Circuits

A New and Innovative Method for CO2 Removal in Anesthetic Circuits: Replacing Chemical Granulate

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03014336
Acronym
memsorb
Enrollment
286
Registered
2017-01-09
Start date
2017-03-20
Completion date
2024-07-24
Last updated
2026-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia

Keywords

co2 removal, anesthesia

Brief summary

The drawbacks of chemical CO2 absorbers include the production of compounds harmful to patients that also lead into increased cost and environmental impact, as well as the daily disposal of compound special waste. Sustainable management of general anesthesia is a growing concern. Continually diluting anesthetic circuits, and the disposal of chemical granulate are serious environmental problems.

Detailed description

DMF Medical has developed a next-generation CO2 filter in order to address the safety issues with current chemical CO2 absorbers in anesthesia. memsorb uses patented advanced medical membrane technology to filter CO2 from anesthetic circuits rather than absorbing via a chemical reaction. This game changing technology relies on a polymeric membrane core (similar to the ones used in oxygenators for cardiac surgery) that selectively allows CO2 to leave the rebreathing system, while maintaining the anesthetic vapor in the circuit. memsorb is a cartridge similar in size and shape to current solutions that simply clicks in place.

Interventions

DEVICEmemsorb

memsorb is a CO2 filter replacing current chemical CO2 absorbers

Sponsors

DMF Medical Incorporated
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* American Society of Anesthesiologists Physical Status Class I, II, III (low-medium risk patient) * English-speaking patients

Exclusion criteria

* Self-reported as pregnant * American Society of Anesthesiologists Physical Status Class IV (high risk patient) * Patients scheduled for emergency surgery * Documented respiratory disease, including COPD and severe asthma * Documented elevated pressure in the brain (intra cranial pressure, ICP)

Design outcomes

Primary

MeasureTime frameDescription
End-tidal CO2 Concentration (%)From the start to the end of the intra-operative period for each participantThe mean concentration of carbon dioxide during the expiratory cycle, measured as a percentage (%), measured over the course of the surgical procedure.

Countries

Canada

Contacts

PRINCIPAL_INVESTIGATOROrlando Hung, MD

Nova Scotia Health Authority

Baseline characteristics

Characteristic
Age, Customized
≥ 18 years
286 participants
Race and Ethnicity Not Collected0 Participants
Sex: Female, Male
Female
55 Participants
Sex: Female, Male
Male
144 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 1110 / 175
other
Total, other adverse events
0 / 1110 / 175
serious
Total, serious adverse events
0 / 1110 / 175

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026