An observational study in Thrombopenia and Central Venous Catheter Placement, sponsored by University Hospital, Angers. Status unknown at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-09-20.
Sponsored by University Hospital, Angers · Observational
PLATCAT study's purpose is to evaluate platelet kinetics after platelet transfusion
703 studies on the registry are indexed under Thrombocytopenia; 150 are open to participants now.
This study's planned enrollment of 30 is below the median of 120 across 186 observational studies indexed under Thrombocytopenia.
Browse Thrombocytopenia studies →University Hospital, Angers is the lead sponsor of 477 studies on the registry; 119 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Haematology patients who needs a central venous catheter and with a non-auto immune thrombopenia
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Prophylactic platelet transfusion in thrombocytopenic patients for the placement of a central venous catheter
72 hours thrombocythemia kinetics after a platelet transfusion
Blood drawing a H-1:00, H+0:10, H+1:00, H+4:00, H+24h00, H+72:00 Evaluation of platelets count on sodium citrate tube.
Time frame: 72 hours post transfusion
Transfusion Safety - assessed by Troubles during process
Troubles during process (pneumothorax, laying failure, hematoma) Hematoma at H+24:00 Immunisation anti HLA,HPA
Time frame: One day after transfusion
Transfusion Efficacy
Number of blood or platelets transfusion
Time frame: One month after transfusion
Description of patients treatment
Type of received chemotherapy
Time frame: One week before and one month after transfusion
Plan to share: No
No publications or documents are linked to this record.
The record gives a start of Jun 2016, a primary completion of Jul 2017 and a completion of Jul 2017. It does not say whether these dates are actual or estimated.
How these figures are worked out, and which studies are left out of them.
This study is status unknown, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.