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Randomized, controlled laboratory investigation.
This prospective, randomized, controlled laboratory study was conducted in 42 Wistar rats.
In a prospective randomized, controlled laboratory study, 14 fasted, anaesthetised, mechanically ventilated animals (22.9 ± 2.8 kg) received 0.75 g/kg body weight faeces into the abdominal cavity to induce sepsis and were observed over 6 hours.
The present study was conducted as a prospective, randomized, controlled laboratory experiment to compare the effects of AVP and TP on Qma and mortality in an established model of ovine septic shock.
The current study was therefore conducted as a prospective, randomized, controlled laboratory experiment to clarify whether and how TEA affects the pulmonary endothelial dysfunction typically seen in the presence of sepsis.
The present study was designed as a prospective, randomized, controlled laboratory experiment to elucidate the effects of AVP and TP (when given as first-line therapy) on mesenteric blood flow (Qma) and mortality in an established model of ovine septic shock.
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A prospective randomized, controlled animal laboratory study in a university animal laboratory.
This was a prospective randomized, controlled animal laboratory study.
This was a large, prospective, randomized controlled trial in a non-laboratory setting.
LDX was effective for up to 13 hours in a phase 3, randomized, controlled trial in children in a laboratory classroom study [ 49].
Randomised controlled trial OR randomized controlled trial.
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