Trial · NCT04713709
Registered outcomes25
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 20 of 25
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Unconjugated naloxone in plasma - Cmax | 0 to 8 hours post dose | Pharmacokinetic Parameters |
| Primary | Unconjugated naloxone in plasma - AUC | 0 to 8 hours post dose | Pharmacokinetic Parameters |
| Primary | Unconjugated naloxone in plasma - Tmax | 0 to 8 hours post dose | Pharmacokinetic Parameters |
| Primary | Unconjugated naloxone in plasma - K el | 0 to 8 hours post dose | Pharmacokinetic Parameters |
| Primary | Unconjugated naloxone in plasma- T half | 0 to 8 hours post dose | Pharmacokinetic Parameters |
| Secondary | Blood pressure | pre-dose | Safety Monitoring: Vital signs |
| Secondary | Pulse | pre-dose | Safety Monitoring: Vital signs |
| Secondary | Blood pressure | 1 hour post dose | Safety Monitoring: Vital signs |
| Secondary | Pulse | 1 hour post dose | Safety Monitoring: Vital signs |
| Secondary | Blood pressure | 2 hour post dose | Safety Monitoring: Vital signs |
| Secondary | Pulse | 2 hour post dose | Safety Monitoring: Vital signs |
| Secondary | Blood pressure | 4 hour post dose | Safety Monitoring: Vital signs |
| Secondary | Pulse | 4 hour post dose | Safety Monitoring: Vital signs |
| Secondary | Blood pressure | 12 hour post dose | Safety Monitoring: Vital signs |
| Secondary | Pulse | 12 hour post dose | Safety Monitoring: Vital signs |
| Secondary | 12-Lead ECG | pre-dose | Safety Monitoring |
| Secondary | 12-Lead ECG | 0.5 hours | Safety Monitoring |
| Secondary | 12-Lead ECG | 2 hours | Safety Monitoring |
| Secondary | 12-Lead ECG | 12 hours | Safety Monitoring |
| Secondary | 4-item NHANES Pocket Smell Test | pre-dose | Safety Monitoring |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT04713709/registered