0 Valutazioni
ID

23180

Descrizione

Responsible Party: Michael Zoller MD, senior physician, Ludwig-Maximilians - University of Munich ClinicalTrials.gov Identifier: NCT01793012 History of Changes Other Study ID Numbers: MUC 428-12 DRKS00004426 ( Other Identifier: German clinical trials register ) Study First Received: January 24, 2013 Last Updated: March 30, 2015 Drug Monitoring of Antibiotics in Critical Care Patients (DRAK) ODM derived from: https://clinicaltrials.gov/ct2/show/NCT01793012

collegamento

https://clinicaltrials.gov/ct2/show/NCT01793012

Keywords

versioni (1)
  1. 26/06/17 26/06/17 -
Caricato su

26 giugno 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Torna ai commenti del modello
Commenti del gruppo di articoli per :

Commenti dell'articolo per :

  • i più nuovi
  • i più vecchi
  • Popolare
  • i più nuovi
    • i più nuovi
    • i più vecchi
    • Popolare

    Non ci sono commenti

    Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

    Eligibility Antibiotics in Critical Care Patients DRKS00004426 NCT01793012 DRKS00004426

    Inglese

    Eligibility Antibiotics in Critical Care Patients NCT01793012 DRKS00004426

    1 moduli  
    Inclusion Criteria
    Descrizione

    Inclusion Criteria

    Alias
    UMLS CUI-1
    C1512693
    0. 18 Years and older (Adult, Senior)
    Descrizione

    Age

    Tipo di dati

    boolean

    1. Hospitalisation in the critical care unit of the Department of Anaesthesiology of the University Hospital of Munich
    Descrizione

    Hospitalization: Critical Care Unit

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0019993
    UMLS CUI [1,2]
    C0021708
    2. Presence of infection by clinical assessment
    Descrizione

    Infection

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0009450
    3. Treatment of the patients with one or more of the following antibiotics: piperacillin/tazobactam, cefepime, meropenem, ciprofloxacin, linezolid, colistin
    Descrizione

    Antibiotics

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0003232
    4. Bolus administration of selected antibiotics
    Descrizione

    Administration Route

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0013153
    5. Valid informed consent subscribed by the patient or by his or her legal guardian or - if only a provisional guardian is defined - by the provisional guardian.
    Descrizione

    Informed Consent

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Descrizione

    Exclusion Criteria

    Alias
    UMLS CUI-1
    C0680251
    0. Healthy Volunteers
    Descrizione

    Control Group

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0009932
    1. Prophylactic antibiotics without clinical assessment for the presence of infection
    Descrizione

    Prophylactic antibiotics

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C1388076
    2. Planned shorter hospital stay than 4 days
    Descrizione

    Hospital Stay

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C3489408
    3. Administration of the selected antibiotic 14 days to 48 hours before the begin of the study
    Descrizione

    Time of Administration

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C1317775
    4. Only a single dose of an antibiotic per day
    Descrizione

    Single Dose

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C1960417
    5. Subsequent withdrawal of the participation in the study by the patient or the guardian
    Descrizione

    Withdrawal

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C2349954
    Ritorna all'inizio della pagina

    Similar models

    Eligibility Antibiotics in Critical Care Patients NCT01793012 DRKS00004426

    1 moduli
    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    Inclusion Criteria
    C1512693 (UMLS CUI-1)
    Age
    Item
    0. 18 Years and older (Adult, Senior)
    boolean
    Hospitalization: Critical Care Unit
    Item
    1. Hospitalisation in the critical care unit of the Department of Anaesthesiology of the University Hospital of Munich
    boolean
    C0019993 (UMLS CUI [1,1])
    C0021708 (UMLS CUI [1,2])
    Infection
    Item
    2. Presence of infection by clinical assessment
    boolean
    C0009450 (UMLS CUI [1])
    Antibiotics
    Item
    3. Treatment of the patients with one or more of the following antibiotics: piperacillin/tazobactam, cefepime, meropenem, ciprofloxacin, linezolid, colistin
    boolean
    C0003232 (UMLS CUI [1])
    Administration Route
    Item
    4. Bolus administration of selected antibiotics
    boolean
    C0013153 (UMLS CUI [1])
    Informed Consent
    Item
    5. Valid informed consent subscribed by the patient or by his or her legal guardian or - if only a provisional guardian is defined - by the provisional guardian.
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    Exclusion Criteria
    C0680251 (UMLS CUI-1)
    Control Group
    Item
    0. Healthy Volunteers
    boolean
    C0009932 (UMLS CUI [1])
    Prophylactic antibiotics
    Item
    1. Prophylactic antibiotics without clinical assessment for the presence of infection
    boolean
    C1388076 (UMLS CUI [1])
    Hospital Stay
    Item
    2. Planned shorter hospital stay than 4 days
    boolean
    C3489408 (UMLS CUI [1])
    Time of Administration
    Item
    3. Administration of the selected antibiotic 14 days to 48 hours before the begin of the study
    boolean
    C1317775 (UMLS CUI [1])
    Single Dose
    Item
    4. Only a single dose of an antibiotic per day
    boolean
    C1960417 (UMLS CUI [1])
    Withdrawal
    Item
    5. Subsequent withdrawal of the participation in the study by the patient or the guardian
    boolean
    C2349954 (UMLS CUI [1])
    Ritorna all'inizio della pagina 

    Aiuto

    Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

    Watch Tutorial