CompletedN/Aketamine

Perioperative Opioid-induced Hyperalgesia and Its Prevention With Ketamine and Methadone

Sponsored by Fondazione IRCCS Istituto Nazionale dei Tumori, Milano

NCT ID
NCT01594047
Target Enrollment
113 participants
Start Date
2009-12-01
Est. Completion
2014-08-01

About This Study

Background: In perioperative period inhibition of N-Methyl-D-Aspartate receptor prevents opioid-induced hyperalgesia and reduce postoperative opioid requirement after abdominal surgery. Methadone is both a µ-opioid receptor agonist like Morphine and a N-Methyl-D-Aspartate antagonist. Study Aim. To evaluate the efficacy of intraoperative Ketamine and postoperative Methadone analgesia in preventing opioid-induced hyperalgesia after abdominal surgery.

Conditions Studied

Post Operative PainHyperalgesia

Interventions

  • ketamine infusion
  • Methadone PCA

Eligibility

Age:18 Years - 75 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* patients undergoing open colo-rectal surgery

Exclusion Criteria:

* ASA status more than II, history of chronic pain, ischemic heart disease or chronic pulmonary disease, allergy to any drugs used in the protocol. Body Max Index more than 35.

Study Locations (1)

Fondazione IRCCS Istituto Nazionale dei Tumori
Milan, Italy

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