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Naloxone for In-Hospital Cardiac Arrest

Naloxone for In-Hospital Cardiac Arrest

Status
Not yet recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07806565
Acronym
naloxone-IHCA
Enrollment
850
Registered
2026-09-08
Start date
2027-01-01
Completion date
2031-07-01
Last updated
2026-09-08

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

Conditions

Heart Arrest

Keywords

naloxone, in-hospital cardiac arrest

Brief summary

The goal of this clinical trial is to learn if the drug naloxone in addition to cardiopulmonary resuscitation improves outcomes of in-hospital cardiac arrets. The main questions it aims to answer are: Does naloxone improve survival after the cardiac arrest? Does naloxone improve functional outcome in survivors of cardiac arrest? Does naloxone improve health related quality of life after the cardiac arrest? How common are adverse reactions to naloxone when administered during cardiopulmonary resuscitation. Researchers will compare naloxone to a placebo (a look-alike substance that contains no drug) to see if naloxone works during cardiac arrest.

Interventions

DRUGnaloxone

2 mg naloxone administered intravenously or intraosseously

DRUGPlacebo

0.9% saline administered intravenously or intraosseously

Sponsors

Region Skane
Lead SponsorOTHER
Lund University
CollaboratorOTHER
Clinical Studies Sweden - Forum South
CollaboratorUNKNOWN
Copenhagen Trial Unit, Center for Clinical Intervention Research
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. In-Hospital Cardiac Arrest 2. Age ≥ 18 years 3. Received at least one dose of adrenaline during CPR

Exclusion criteria

1. "Do-not-resuscitate"-order 2. Known/suspected pregnancy 3. Known objection by the patient to participate in the trial 4. Previous inclusion in the trial

Design outcomes

Primary

MeasureTime frameDescription
30-day survival30 days after the cardiac arrestproportion of patients alive

Contacts

CONTACTAnna Lybeck, MD PhD
anna.lybeck@med.lu.se0771-11 14 44

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 9, 2026