Last reviewed · How we verify
NCT07471555: IO_nursing
Vascular Access and Intraosseus
NA trial testing Epinephrine Ampoule (Manual Preparation) in To Compare the Time Required to Administer 1 mg of Epinephrine, as Well as the Total Procedure in 52 participants. Enrolling by invitation.
3 April 2026
Quick facts
| Lead sponsor | University of Valencia |
|---|---|
| Phase | NA |
| Status | ENROLLING BY INVITATION |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | supportive care |
| Enrollment | 52 |
| Start date | 2 April 2026 |
| Primary completion | 3 April 2026 |
| Estimated completion | 3 December 2026 |
| Sites | 1 location across Spain |
Drugs / interventions tested
- Epinephrine Ampoule (Manual Preparation)
- Epinephrine Prefilled Syringe (Ready-to-use)
- Intravenous (IV) Access
- Intraosseous (IO) Access Device
Conditions studied
- To Compare the Time Required to Administer 1 mg of Epinephrine, as Well as the Total Procedure — all drugs for To Compare the Time Required to Administer 1 mg of Epinephrine, as Well as the Total Procedure →
Sponsor
University of Valencia
Who can join
18 and older, any sex, with To Compare the Time Required to Administer 1 mg of Epinephrine, as Well as the Total Procedure. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Rapid administration of epinephrine is an essential component of advanced life support during cardiac arrest. Peripheral intravenous (IV) access is commonly used for drug delivery, while intraosseous (IO) access is an alternative when IV access is not readily available. In addition, epinephrine may be administered using different drug presentations, such as ampoules or prefilled syringes, which may influence procedural workflow during resuscitation.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07471555
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07471555 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Valencia
- Last refreshed: 13 March 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07471555.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing