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NCT04368000: PAPR
Prone Positioning in Awake Patients With COVID-19 Requiring Hospitalization
NA trial testing Intermittent prone positioning instructions in Respiratory Failure in 30 participants. Terminated before completion.
6 August 2020
Quick facts
| Lead sponsor | University of Utah |
|---|---|
| Phase | NA |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 30 |
| Start date | 29 April 2020 |
| Primary completion | 6 August 2020 |
| Estimated completion | 6 August 2020 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Intermittent prone positioning instructions
- Usual care positioning with no instructions
Conditions studied
- Respiratory Failure — all drugs for Respiratory Failure →
- COVID-19 — all drugs for COVID-19 →
Sponsor
University of Utah
Who can join
18 and older, any sex, with Respiratory Failure or COVID-19. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Acute respiratory distress syndrome (ARDS) is a major complication among patients with severe disease. In a report of 138 patients with COVID-19, 20% developed ARDS at a median of 8 days after the onset of symptoms, with 12.3% of patients requiring mechanical ventilation. Efficacious therapies are desperately needed. Supportive care combined with intermittent prone positioning may improve outcomes. Prone positioning (PP) of patients with severe ARDS (when combined with other lung-protective ventilation strategies) is associated with a significant mortality benefit. In addition, PP for \>12 hours in severe ARDS is strongly recommended by clinical practice guidelines. The aim of this study is to compare the outcomes of prone positioning versus usual care positioning in non-intubated patients hospitalized for COVID-19.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Patient-directed Prone Positioning in Awake Patients with COVID-19 Requiring Hospitalization (PAPR).
Johnson SA, Horton DJ, Fuller MJ, Yee J, et al · · 2021 · cited 46× · PMID 33596394 · DOI 10.1513/annalsats.202011-1466rl -
Outcomes Evaluated in Controlled Clinical Trials on the Management of COVID-19: A Methodological Systematic Review.
Mathioudakis AG, Fally M, Hashad R, Kouta A, et al · · 2020 · cited 14× · PMID 33333777 · DOI 10.3390/life10120350
Verify or expand the search:
- PubMed search for NCT04368000
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT04368000 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- 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 Utah
- Last refreshed: 3 December 2020
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/NCT04368000.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing