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Intranasal Ketamine for Procedural Sedation in Pediatric Laceration Repair

NCT00451724 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2010-07-22

No results posted yet for this study

Summary

The purpose of this study is to compare how well three different doses of ketamine, given as a spray into the nose, help to sedate children and help them tolerate repairs of cuts on their faces.

Conditions

  • Laceration

Interventions

DRUG

Intranasal ketamine

Sponsors & Collaborators

  • Rhode Island Hospital

    lead OTHER

Principal Investigators

  • James G Linakis, PhD, MD · Rhode Island Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
1 Year
Max Age
7 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-05-31
Completion
2010-02-28

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00451724 on ClinicalTrials.gov