Opioid-Induced Respiratory Depression: Naloxone and Nalmefene Study
We are studying how well naloxone and nalmefene can reverse breathing problems caused by opioids in both new and long-term users. This research aims to improve treatment options for respiratory depression in real-life settings.
What diseases are being studied?
Health conditions and diseases that the clinical trial is designed to study and treat.
Opioid Use Disorder
Opioid Use Disorder (OUD) is a medical condition characterized by a problematic pattern of opioid use, leading to significant impairment or distress, including cravings and withdrawal symptoms.
Who can participate in the clinical trial?
These questions help us understand your situation so we can let the trial team know whether you might be a potential match. This is not a medical evaluation and is not part of the official screening, the study doctor will make the final decision..
- Are you between 18 and 70 years old?
- Do you have a history of substance use disorder (like addiction to drugs or alcohol)?
- Are you currently pregnant or breastfeeding?
- Have you had major surgery or a significant injury in the past 4 weeks?
- Are you taking any medications for opioid use disorder?
What experimental substances are being tested?
Experimental substances that are being investigated in this clinical trial. These are not yet approved for general use.
What similar medicines might you know?
Don't worry if you don't know the medicines tested in the trial. There is a chance you have heard about the similar medicines. Check the list below to see if you are familiar with any of them.
Where is the clinical trial being conducted?
Locations and medical facilities where this clinical trial is currently recruiting or conducting research. Select the locations where you would like to participate.
Disclaimer: Parts of this content have been automatically extracted from the EU Clinical Trials registry. While we strive for accuracy, please always contact the trial site or sponsor directly for correct and official information before making any decisions about participation. View on EU Clinical Trials.