CompletedPhase 4ketamine

Ketamine vs Hydromorphone

Sponsored by University of Florida

NCT ID
NCT03001843
Target Enrollment
54 participants
Start Date
2017-02-22
Est. Completion
2018-12-21

About This Study

This study will help to determine if investigators can minimize narcotic use in laparoscopic gastric bypass patients while maintaining adequate pain control. This will allow investigators to minimize the negative side effects of narcotics which is a goal in this population.

Conditions Studied

Laparoscopic Gastric BypassObesityPain, Postoperative

Interventions

  • Ketamine
  • Narcotics
  • pain scale

Eligibility

Age:18 Years - 65 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Obese patient presenting for laparoscopic gastric bypass between 18 and 65 years of age

Exclusion Criteria:

* Hypersensitivity, allergy, or contraindications to fentanyl, propofol, or ketamine.

Study Locations (1)

University of Florida
Gainesville, Florida, 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