CompletedPhase 4ketamine

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

Sponsored by Asker & Baerum Hospital

NCT ID
NCT00354029
Target Enrollment
83 participants
Start Date
2006-08
Est. Completion
2009-05

About This Study

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.

Conditions Studied

HemorrhoidsPain

Interventions

  • S (+) Ketamine
  • Placebo

Eligibility

Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

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

Exclusion Criteria:

* Age \< 18
* ASA \> II
* liver failure
* renal failure
* heart failure
* glaucoma
* pregnancy

Study Locations (1)

Asker and Baerum Hospital
Rud, Norway

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source