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Expanded Access for Inhaled Isoflurane Delivered Via the Sedaconda ACD-S for Sedation of Difficult-to-Sedate Adult Mechanically Ventilated Intensive Care Unit Patients

Expanded Access for Inhaled Isoflurane Delivered Via the Sedaconda ACD-S for Sedation of Difficult-to-Sedate Adult Mechanically Ventilated Intensive Care Unit Patients

Status
AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT07457593
Enrollment
Unknown
Registered
2026-03-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Sedation

Keywords

inhaled sedation, Sedaconda ACD-S, Difficult to sedate, Sedana Medical, Sedana

Brief summary

The purpose of this Expanded Access Protocol is to provide access to inhaled isoflurane delivered via the Sedaconda ACD-S device for sedation of adult patients in the ICU that are mechanically ventilated and are difficult to sedate with current available treatment options, and who, in the opinion of their treating physician, would benefit from this treatment.

Interventions

DRUGIsoflurane

Isoflurane for inhaled sedation

DEVICESedaconda ACD-S

Sedaconda ACD-S is a medical device which enables the administration of volatile anesthetics (isoflurane)

Sponsors

Sedana Medical
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Adults ≥18 years of age; * Receiving invasive mechanical ventilation and continuous sedation in the ICU; * Inability to maintain a target sedation level ensuring patient comfort and safety with conventional intravenous sedatives, in clinically appropriate combinations and at maximum tolerated doses, despite optimized analgesia and ventilator settings, with 1. recurring episodes of agitation or self-harm, such as attempting or actual removal of an endotracheal tube or of indwelling catheters or monitors, or necessitating physical restraints; or 2. escalating sedative and opioid drug doses, despite mitigating strategies (e.g., sedative drug combinations or rotation to reduce toxicity); or 3. clinical concerns for, or indications of, serious untoward effects of ongoing conventional intravenous sedation and analgesia agents (e.g., hypertriglyceridemia, propofol-related infusion syndrome, bradycardia, iatrogenic withdrawal syndrome); and * No other available sedative option is considered appropriate * Is not currently enrolled in or is eligible for a clinical study that would prohibit the participation in this EAP.

Exclusion criteria

* Ventilator tidal volume \<200 or \>1000 mL * Need for high frequency oscillation ventilation (HFOV) or high frequency percussive ventilation (HFPV) * Comfort care only (end of life care); * Suspected but unmonitored elevated intracranial pressure (e.g., patients with acute stroke, severe head trauma, meningitis without ICP monitoring); * Contraindication to isoflurane, including: 1. Known or suspected personal or family history of malignant hyperthermia (MH) or high risk for MH or acute drug-induced muscle injury (eg, muscular dystrophies); 2. Severe hemodynamic compromise; 3. Known hypersensitivity reaction to isoflurane or other halogenated volatile anesthetic agents * History of ventricular tachycardia/Long QT Syndrome; * Female patients who are pregnant or breast-feeding; * Imperative need for continuous active humidification through mechanical ventilation circuit; * Any medical conditions, that, in the Investigator´s opinion, would impose excessive risk to the patient or would adversely affect the patient's participation in the EAP; * Inability to obtain informed consent.

Contacts

CONTACTIda Sverud, MSc
medinfo@sedanamedical.com+46 8 124 05 200
CONTACTPeter Sackey, MD, PhD, DESA, EDIC
medinfo@sedanamedical.com+46 8 124 05 200

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026