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 |