Phase 4
Completed N=83
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
| Outcome | Result | p-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
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.