​​​​ATTIRE Randomised Clinical Trial

Data Collection: 


Data collection can be divided into: 

  1. Screening 
  2. Day 1 treatment
    • Reason for admission, co-morbidities
    • Current treatment, blood test results
    • Vital signs from observation chart
    • IV fluid and albumin administration
    • Evidence of infection and medications prescribed
  3. Day 2-14 (or discharge) 
    • Patient location
    • Current treatment, blood test results
    • Vital signs from observation chart (worst in previous 24 hours)
    • IV fluid and albumin administration
    • ATTIRE CRF Completion Guidelines v2.0 08Jan2016 (pp).pdf
  4. Infection
    • Reason for diagnosis
  5. Quality of Life Questionnaires
    • CSRI: Admission, discharge and follow up
    • EQ-5D-5L: Admission, discharge and follow up


The data to be recorded should almost entirely be from the patients notes, vital signs chart and computer laboratory data


At the end of the patient's trial period the CRFs should be scanned and sent (encripted email) to UCL CTU for entry to the database - as detailed in CRF completion guidance document.