CompletedPhase 4ketamine

Analgesia During Pediatric Digestive Endoscopy: a Comparison of Two Protocols for Procedural Sedation

Sponsored by Université de Montréal

NCT ID
NCT01168492
Target Enrollment
90 participants
Start Date
2010-07
Est. Completion
2013-07

About This Study

The purpose of this study is to determine whether ketamine, midazolam, and meperidine are more effective than midazolam and meperidine alone for procedural sedation and analgesia in pediatric digestive endoscopy. Secondary outcomes are the incidence of cardiorespiratory side effects and the necessity of rescue doses.

Conditions Studied

Pain

Interventions

  • ketamine

Eligibility

Age:10 Years - 19 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Children =/\> 10 years of age
* Undergoing elective diagnostic colonoscopy
* ASA score class 1-3.

Exclusion Criteria:

* Children younger than 10 years of age
* Known epilepsy under treatment
* ASA score class 4 or more
* Interventional colonoscopy (e.g.polypectomy)

Study Locations (1)

Sainte Justine Hospital
Montreal, Quebec, Canada

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