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Phase 4 Completed N=83 Randomized Quadruple-blind Treatment

Effect of Perioperative i.v. Low-dose S(+) Ketamine

Source: ClinicalTrials.gov NCT00354029 ↗
Enrolled (actual)
83
Serious AEs
0.0%
Results posted
Jul 2011
Primary outcomePrimary: NRS Pain = Numeric Rating Scale (0-10) — 1.6; 1.5 Units on a scale — p=>0.05

Summary

The purpose of this study is to determine whether the use of perioperative intravenous S (+) ketamine reduces the amount and degree of postoperative pain. Furthermore the purpose of this study is to determine whether the use of perioperative intravenous S (+) ketamine effects cognitive function in the early postoperative period.

Outcome Measures

OutcomeResultp-value
PRIMARY
NRS Pain = Numeric Rating Scale (0-10)
1.6; 1.5 >0.05

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of disc prolapse
  • Age 18+
  • ASA (American Society in Anesthesiology) I-II
  • written consent

Exclusion Criteria

  • Age II
  • liver failure
  • renal failure
  • heart failure
  • glaucoma
  • pregnancy
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00354029). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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