- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00656396
Point of Care Coagulation Testing in Patients Undergoing Major Surgery (POC-OP)
7. september 2015 opdateret af: University of Bern
Does Point of Care Coagulation Testing Reduce the Transfusion of Non-erythrocyte Blood Products in Patients Undergoing Major Surgery? A Randomized-Controlled Trial
Bleeding is a frequent complication during surgery.
The peri-operative administration of blood products, including packed red blood cells, thrombocytes and fresh frozen plasma (FFP), is often deemed necessary.
Therefore the transfusion of allogenic blood products mandates strategies to optimize the clinical decision to transfuse.
The decision to administer FFP is usually made in the absence of any data.
Point of care testing of prothrombin time ensures that a major parameter of coagulation is readily available.
The test is fast, easy to perform, inexpensive and may enable physicians to rationally determine the need for FFP.
Objective of the study is to determine the effectiveness of point of care coagulation testing of prothrombin time to reduce the administration of FFP.
Studieoversigt
Status
Afsluttet
Betingelser
Detaljeret beskrivelse
Background: Bleeding is a frequent complication during surgery.
The peri-operative administration of blood products, including packed red blood cells, thrombocytes and fresh frozen plasma (FFP), is often deemed necessary.
Beside the expenses of blood products these products carry risks of infection, allergic reaction and immune-modulation.
Therefore the transfusion of allogenic blood products mandates strategies to optimize the clinical decision to transfuse.
Bleeding during surgery is a dynamic process; it can happen within minutes and result not only in major blood loss, but also in coagulation aberrations.
The indication for a transfusion should be based on reliable coagulation studies.
Traditional coagulation studies require up to 1 hour.
Therefore, the decision to administer FFP is usually made in the absence of any data.
Point of care testing of prothrombin time ensures that a major parameter of coagulation is readily available in the operation theatre within 3 minutes.
It is fast, easy to perform, inexpensive and may enable physicians to rationally determine the need for FFP.
Objective: To determine the effectiveness of point of care coagulation testing of prothrombin time to reduce the administration of FFP.
Methods: Patient and assessor blind, single center randomized controlled parallel group trial in 220 patients aged between 18 and 90 years undergoing major surgery (any type, except cardiac surgery and liver transplant) with an estimated blood loss during surgery exceeding 20% of the calculated normal total blood volume or a requirement of FFP according to the judgment of treating surgeons or anesthesiologists.
Patients will be randomized to usual care plus point of care coagulation testing or usual care alone without point of care testing.
Primary endpoint will be the relative risk to receive any FFP peri-operatively.
Significance: Point of care coagulation testing in the operation theatre may reduce the administration of fresh frozen plasma considerably, which in turn may decrease costs and complications usually associated with the administration of allogenic blood products.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
228
Fase
- Fase 3
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Bern, Schweiz, 3010
- University Hospital Bern
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år til 90 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Age between 18 and 90 years
- Major surgery
- Estimated blood loss during surgery > 20% of individual blood volume of 70ml per kg body weight
- Patients requiring FFP
Exclusion Criteria:
- Known hereditary coagulopathy
- Liver transplant
- Cardiac surgery
- Pregnancy
- Preoperative hemoglobin <100g/l
- Abnormal coagulation studies before surgery
- Active treatment with drugs inhibiting coagulation or platelet function
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Sundhedstjenesteforskning
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Aktiv komparator: Kontrollere
Standardpleje
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Standard care
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Eksperimentel: Intervention
Point of care monitoring used
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Coagucheck XS Plus® is used for intraoperative measurement of Prothrombin time
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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The relative risk to receive any FFP peri-operatively.
Tidsramme: at post-operative discharge from hospital, estimated to be about 5 days after randomisation
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at post-operative discharge from hospital, estimated to be about 5 days after randomisation
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Number of units of FFP received between randomization and post-operative discharge from hospital
Tidsramme: at post-operative discharge from hospital, estimated to be about 5 days after randomisation
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at post-operative discharge from hospital, estimated to be about 5 days after randomisation
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The relative risk of major in-hospital bleeding defined as bleeding event requiring an extension of hospitalization, reoperation due to bleeding, bleeding resulting in hemorrhagic shock or death
Tidsramme: at post-operative discharge from hospital, estimated to be about 5 days after randomisation
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at post-operative discharge from hospital, estimated to be about 5 days after randomisation
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The relative risk of an APTC event (non-fatal myocardial infarction, non-fatal stroke, cardiovascular death, or death of unknown cause) between randomization and post-operative discharge from hospital
Tidsramme: at post-operative discharge from hospital, estimated to be about 5 days after randomisation
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at post-operative discharge from hospital, estimated to be about 5 days after randomisation
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The relative risk of overall mortality between randomization and post-operative discharge from hospital
Tidsramme: at post-operative discharge from hospital, estimated to be about 5 days after randomisation
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at post-operative discharge from hospital, estimated to be about 5 days after randomisation
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Studieleder: Robert Greif, MD MME, Departement of Anesthesiology and Pain Therapy, Bern University Hospital
- Ledende efterforsker: Natalie Urwyler, MD, Bern University Hospital
- Studiestol: Peter Jüni, PD Dr med, CTU Bern, Bern University Hospital, and Institute of Social and Preventive Medicine, University of Bern
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. maj 2008
Primær færdiggørelse (Faktiske)
1. september 2011
Studieafslutning (Faktiske)
1. september 2011
Datoer for studieregistrering
Først indsendt
7. april 2008
Først indsendt, der opfyldte QC-kriterier
10. april 2008
Først opslået (Skøn)
11. april 2008
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
9. september 2015
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
7. september 2015
Sidst verificeret
1. september 2015
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- KEK 232_06
- 232_06 (Anden identifikator: KEK)
- 3200B0_122461 (Andet bevillings-/finansieringsnummer: SNF)
- 1295 (Inselspital)
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .