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Table 2 Prior probability estimates and calculated chances of a true positive result for each trial

From: Effect sizes in ongoing randomized controlled critical care trials

Trial name

Prior probability estimatesa (%)

Chance of a true-positiveb (%)

 

Median estimate (IQR)

Range of estimates

Median calculated chance (IQR)

Range of calculated chances

A Confirmatory Phase II/III Study Assessing Efficacy, Immunogenicity and Safety of IC43 Recombinant Pseudomonas Vaccine in Intensive Care Patients

5 (0.33–20)

0–82

49 (6–82)

0–99

ADjunctive coRticosteroid trEatment iN criticAlly ilL Patients with Septic Shock

20 (5–50)

0–100

82 (49–95)

0–100

Early Spontaneous Breathing in ARDS

10 (1–25)

0–100

64 (14–84)

0–100

Non-sedation versus Sedation with a Daily Wake-up Trial in Critically Ill Patients Receiving Mechanical Ventilation

20 (5–40)

0–100

80 (46–91)

0–100

Stress Ulcer Prophylaxis in the Intensive Care Unit

10 (0.030–28.75)

0–100

67 (1–88)

0–100

The Augmented versus Routine Approach to Giving Energy Trial

10 (2–40)

0–90

64 (29–91)

0–99

The SuDDICU Cluster RCT of Antibiotic Prophylaxis in Critical Illness

25 (10–50)

0–100

86 (67–95)

0–100

Ticagrelor in Severe CAP

2.5 (0–10)

0–100

29 (0–64)

0–100

Tranexamic acid for the treatment of gastrointestinal haemorrhage: an international randomised, double-blind, placebo-controlled trial

35 (10–57.5)

0–100

91 (67–96)

0–100

Tranexamic acid for the treatment of significant traumatic brain injury: an international, randomised, double-blind, placebo-controlled trial

20 (10–50)

0–100

82 (67–95)

0–100

  1. Abbreviations: APRV Airway pressure release ventilation, ARDS Acute respiratory distress syndrome, CAP Community-acquired pneumonia, GI Gastrointestinal, ICU Intensive care unit, IQR Interquartile range, SDD Selective digestive decontamination, RRT Renal replacement therapy
  2. aPrior probability was defined as the percentage chance, estimated by clinicians, that a trial would demonstrate a mortality effect equal to or greater than that used by the trials investigators in their sample size calculation
  3. bCalculated chances of a true-positive result are based on the prior probabilities shown and assume power (β) specified by the trial investigators and an α of 0.05 using the following calculation: True-positive rate = (prior probability) × β/(1 − prior probability) × α) + (prior probability × β)