HYPOPhosphatemia in the Intensive Care: A One-day Point Prevalence Survey
HYPO-P-ICU
Hypophosphatemia in the ICU - A One-day Point Prevalence Survey
2 other identifiers
observational
890
3 countries
4
Brief Summary
The point prevalence survey aims at defining the until now unknown real prevalence of hypophosphatemia (defined as blood phosphate value \< 0.8 mmol/l) in international critical care settings
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2020
Shorter than P25 for all trials
4 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 14, 2019
CompletedFirst Posted
Study publicly available on registry
December 17, 2019
CompletedStudy Start
First participant enrolled
March 9, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 31, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
July 31, 2020
CompletedFebruary 2, 2021
January 1, 2021
5 months
December 14, 2019
January 31, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Prevalence of hypophosphatemia
Blood value \< 0.8 mmol/l
1 day
Interventions
Phosphate administration (yes or no)
Eligibility Criteria
Critically ill patients: adults and children
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (4)
Tartu University Hospital
Tartu, 50407, Estonia
Hôpital Pasteur 2
Nice, 06000, France
Lausanne University Hospital
Lausanne, Canton of Vaud, 1011, Switzerland
Hôpital de Nyon
Nyon, 1260, Switzerland
Related Publications (1)
Berger MM, Appelberg O, Reintam-Blaser A, Ichai C, Joannes-Boyau O, Casaer M, Schaller SJ, Gunst J, Starkopf J; ESICM-MEN section. Prevalence of hypophosphatemia in the ICU - Results of an international one-day point prevalence survey. Clin Nutr. 2021 May;40(5):3615-3621. doi: 10.1016/j.clnu.2020.12.017. Epub 2020 Dec 29.
PMID: 33454128DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mette M BERGER, MD PhD
Lausanne University Hospital, Lausanne, Switzerland
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
December 14, 2019
First Posted
December 17, 2019
Study Start
March 9, 2020
Primary Completion
July 31, 2020
Study Completion
July 31, 2020
Last Updated
February 2, 2021
Record last verified: 2021-01
Data Sharing
- IPD Sharing
- Will not share
Data will be collected in central REDCap database. No individual patient data will be made available