Clinical Trials Directory

Trials / Completed

CompletedNCT01070108

Escalating Ketamine Doses and Pre-emption

EARLY PREOPERATIVE ESCALATING DOSES OF KETAMINE ATTENUATE POSTOPERATIVE PAIN AND REDUCE MORPHINE CONSUMPTION IN HUMANS

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Tel-Aviv Sourasky Medical Center · Other Government
Sex
All
Age
15 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Ketamine affects postoperative pain when administered intravenously immediately before, during or at the end of surgical procedures. We assessed the effects of multiple and escalating doses of ketamine administered many hours before surgery on postoperative pain and analgesia consumption.

Conditions

Interventions

TypeNameDescription
DRUGKetaminegroup receiving one injection (25 mg) of ketamine (K1) intramuscularly (IM) at 3-4 hours before surgery or placebo (saline 0.9%, NS)
DRUGketamineketamine at 11-12 hours (10 mg) and 3-4 hours (25 mg) before surgery (K2), with a corresponding NS group
DRUGketamineketamine injected IM 17-18, 11-12, and 3-4 hours before surgery (5, 10 and 25 mg, respectively) (K3), and the second group received NS

Timeline

Start date
2007-01-01
Primary completion
2009-01-01
Completion
2009-01-01
First posted
2010-02-17
Last updated
2010-02-17

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01070108. Inclusion in this directory is not an endorsement.