CompletedN/Aketamine

Low Dose Ketamine as an Adjunct to Fentanyl in Outpatient Tonsillectomy

Sponsored by Mayo Clinic

NCT ID
NCT00587665
Target Enrollment
122 participants
Start Date
2006-08
Est. Completion
2007-12

About This Study

Comparing patients receiving subanesthetic doses of Ketamine vs placebo to see if it can reduce narcotic needs for patients receiving a tonsillectomy and adenoidectomy

Conditions Studied

Pain

Interventions

  • •ketamine
  • •Placebo

Eligibility

Age:3 Years - 12 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:between 3 and 12 years of age

* ASA 1 or 2

Exclusion Criteria:

* did not consent

Study Locations (1)

Mayo Clinic
Rochester, Minnesota, United States

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

Low Dose Ketamine as an Adjunct to Fentanyl in Outpatient Tonsillectomy | Huxley