At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 42 enrolled
Drug / intervention
Ketamine +1 moredrug
Likely dose
Ketamine 0.25 mg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Phase 4: Study of Ketamine Inhibition of Interleukin 6 in Hepatic Resections Requiring Temporary Porto-arterial Occlusion
In Brief
A Phase 4 clinical trial evaluating Ketamine and Placebo for Hepatectomy. Completed, enrolled 42 participants across 1 site.
Detailed Summary
The purpose of this study is to determine whether ketamine is effective to inhibit interleukin 6 synthesis in hepatic resections requiring temporary porto-arterial occlusion.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHepatectomy
CountriesArgentina
Collaborators--
Timeline
Phase 4CompletedFinished
200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartJun 2001
Primary CompletionJun 2008
First PostedSep 2009
TodayJul 2026
First PostedSep 17, 2009
Enrollment StartJun 1, 2001
Primary CompletionJun 1, 2008
TodayJul 2, 2026
Enrollment to primary: 7 yearsPosted 16.8 years ago
Interventions
Ketaminedrug
Ketamine: 0.25 mg/kg, intravenously, one dose.
Placeboother
saline solution