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A clinical trial of progesterone for severe traumatic brain injury.

AbstractBACKGROUND:
Progesterone has been associated with robust positive effects in animal models of traumatic brain injury (TBI) and with clinical benefits in two phase 2 randomized, controlled trials. We investigated the efficacy and safety of progesterone in a large, prospective, phase 3 randomized clinical trial.
METHODS:
We conducted a multinational placebo-controlled trial, in which 1195 patients, 16 to 70 years of age, with severe TBI (Glasgow Coma Scale score, ≤8 [on a scale of 3 to 15, with lower scores indicating a reduced level of consciousness] and at least one reactive pupil) were randomly assigned to receive progesterone or placebo. Dosing began within 8 hours after injury and continued for 120 hours. The primary efficacy end point was the Glasgow Outcome Scale score at 6 months after the injury.
RESULTS:
Proportional-odds analysis with covariate adjustment showed no treatment effect of progesterone as compared with placebo (odds ratio, 0.96; confidence interval, 0.77 to 1.18). The proportion of patients with a favorable outcome on the Glasgow Outcome Scale (good recovery or moderate disability) was 50.4% with progesterone, as compared with 50.5% with placebo. Mortality was similar in the two groups. No relevant safety differences were noted between progesterone and placebo.
CONCLUSIONS:
Primary and secondary efficacy analyses showed no clinical benefit of progesterone in patients with severe TBI. These data stand in contrast to the robust preclinical data and results of early single-center trials that provided the impetus to initiate phase 3 trials. (Funded by BHR Pharma; SYNAPSE ClinicalTrials.gov number, NCT01143064.).
AuthorsBrett E Skolnick, Andrew I Maas, Raj K Narayan, Roland Gerritsen van der Hoop, Thomas MacAllister, John D Ward, Neta R Nelson, Nino Stocchetti, SYNAPSE Trial Investigators
JournalThe New England journal of medicine (N Engl J Med) Vol. 371 Issue 26 Pg. 2467-76 (Dec 25 2014) ISSN: 1533-4406 [Electronic] United States
PMID25493978 (Publication Type: Clinical Trial, Phase III, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
Chemical References
  • Progesterone
Topics
  • Adolescent
  • Adult
  • Aged
  • Brain Injuries (drug therapy)
  • Double-Blind Method
  • Drug Administration Schedule
  • Female
  • Glasgow Coma Scale
  • Glasgow Outcome Scale
  • Humans
  • Infusions, Intravenous
  • Intention to Treat Analysis
  • Male
  • Middle Aged
  • Odds Ratio
  • Progesterone (administration & dosage, adverse effects)
  • Treatment Failure
  • Young Adult

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