Staphylococcus Aureus Bacteraemia in Adults
ISAC
A Prospective International Study of Staphylococcus Aureus Bacteraemia in Adults by the International Staphylococcus Aureus Collaboration
1 other identifier
observational
2,000
5 countries
24
Brief Summary
The purpose of this evaluation is to record the management and outcome of adults with S.aureus bacteraemia (SAB) across multiple European, Asian and North American sites and to identify key quality indicators associated with improved outcome.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2013
Typical duration for all trials
24 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2013
CompletedFirst Submitted
Initial submission to the registry
March 25, 2014
CompletedFirst Posted
Study publicly available on registry
March 28, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2016
CompletedDecember 3, 2014
December 1, 2014
2.3 years
March 25, 2014
December 2, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Mortality
90 Days
Secondary Outcomes (1)
Length of hospital stay
90 Days
Eligibility Criteria
Patient in tertiary care hospitals
You may qualify if:
- S. aureus (methicillin sensitive or resistant) isolated from one or more blood cultures
You may not qualify if:
- Recurrent episodes of S. aureus bloodstream infection
- Polymicrobial infection
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (24)
Uniklinik Koln
Cologne, North Rhine-Westphalia, 50935, Germany
Uniklinik Freiburg
Freiburg im Breisgau, 79106, Germany
Univeritatklinikum Schleswig-Holstein
Lübeck, 23562, Germany
Seoul National University Bundang Hospital
Seoul, South Korea
Hospital San Pau
Barcelona, 08026, Spain
University Hospital Clinic de Barcelona
Barcelona, 08028, Spain
Hospital Vall d'Hebron
Barcelona, 08035, Spain
Hospital Universitario Son Espases
Palma. Mallorca, 79 07120, Spain
Salamanca Hospital
Salamanca, Spain
Hospital Universitario Virgen Macarena
Seville, 41007, Spain
Hospital Universitario Virgen del Rocio
Seville, 41013, Spain
Far Eastern Memorial Hospital
New Taipei City, Taiwan
Birmingham Heartlands Hospital
Birmingham, West Midlands, B9 5SS, United Kingdom
Brighton and Sussex University Hospitals
Brighton, BN2 5BE, United Kingdom
Cambridge University Hospitals
Cambridge, CB2 0QQ, United Kingdom
Hull and East Yorkshire Hospitals
Hull, HU3 2JZ, United Kingdom
Royal Liverpool and Broadgreen Hospital
Liverpool, L7 8XP, United Kingdom
Royal Free Hospital
London, NW3 2QG, United Kingdom
Guy's and St Thomas'
London, SE1 7EH, United Kingdom
Kings College Hospital
London, SE5 9RS, United Kingdom
University College London Hospital
London, WC1E 6AG, United Kingdom
Oxford University Hospitals
Oxford, OX3 9DU, United Kingdom
Plymouth Hospitals
Plymouth, PL6 8DH, United Kingdom
Portsmouth Hospitals
Portsmouth, PO3 6AD, United Kingdom
Related Publications (1)
Kaasch AJ, Barlow G, Edgeworth JD, Fowler VG Jr, Hellmich M, Hopkins S, Kern WV, Llewelyn MJ, Rieg S, Rodriguez-Bano J, Scarborough M, Seifert H, Soriano A, Tilley R, Torok ME, Weiss V, Wilson AP, Thwaites GE; ISAC, INSTINCT, SABG, UKCIRG, and Colleagues. Staphylococcus aureus bloodstream infection: a pooled analysis of five prospective, observational studies. J Infect. 2014 Mar;68(3):242-51. doi: 10.1016/j.jinf.2013.10.015. Epub 2013 Nov 16.
PMID: 24247070BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Achim J Kaasch, MD
University of Cologne
Central Study Contacts
Christian M Bernasch
CONTACT
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 3 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr. Achim Kaasch
Study Record Dates
First Submitted
March 25, 2014
First Posted
March 28, 2014
Study Start
January 1, 2013
Primary Completion
May 1, 2015
Study Completion
May 1, 2016
Last Updated
December 3, 2014
Record last verified: 2014-12