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NCT04660448: LUS-PICO
Lung Ultrasound Score and Pediatric Intensive Care Outcomes (LUS-PICO)
trial testing Bedside lung ultrasound examination in Lung Injury in 650 participants. Completed in 30 November 2021.
31 March 2021
Quick facts
| Lead sponsor | Fundación para la Investigación Biosanitaria del Principado de Asturias |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 650 |
| Start date | 1 December 2020 |
| Primary completion | 31 March 2021 |
| Estimated completion | 30 November 2021 |
| Sites | 1 location across Spain |
Drugs / interventions tested
- Bedside lung ultrasound examination
Conditions studied
- Lung Injury — all drugs for Lung Injury →
- Extravascular Lung Water — all drugs for Extravascular Lung Water →
- Pulmonary Edema — all drugs for Pulmonary Edema →
- Acute Respiratory Distress Syndrome — all drugs for Acute Respiratory Distress Syndrome →
Sponsor
Fundación para la Investigación Biosanitaria del Principado de Asturias
Who can join
Adults 1 Month to 18, any sex, with Lung Injury or Extravascular Lung Water. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Bedside lung ultrasonography helps to obtain reliable clinical information about lung aeration, that has been categorized by means of the so-called lung ultrasound score (LUS). In critically ill adults, LUS has been related with the outcome both in patients with respiratory and some non-respiratory conditions. Pediatric studies about lung aeration have been done mainly on postoperative cardiac patients and infants with bronchiolitis. In this prospective, observational, multicenter, feasibility and diagnostic accuracy study, we will explore the degree of lung aeration impairment as a potential outcome predictor in critically ill children with a variety of underlying conditions. Children from 1 month to 18 years of age admitted to PICU will be recruited and LUS will be calculated at two time points: at 12 ± 6 hours and at 48-72 hours. Univariate and multivariate statistical analysis will be performed in order to ascertain the outcome influence of clinical factors in general and LUS in particular.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT04660448
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Trials by the same sponsor.
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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 NCT04660448 (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 Fundación para la Investigación Biosanitaria del Principado de Asturias
- Last refreshed: 12 April 2022
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/NCT04660448.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing