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Effects of Oral Midazolam in Comparison Promethazine With Nitrous Oxide for Uncooperative Children

NCT01118884 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2010-05-07

No results posted yet for this study

Summary

The purpose of this study is to compare the safety and efficacy of sedation using orally administered midazolam and promethazine with nitrous oxide/oxygen in uncooperative children receiving dental treatments.

Conditions

  • Conscious Sedation

Interventions

DRUG

Promethazine

Syrup ,1 mg/kg, oral , 30 minutes before dental procedure , its duration is 4-6 hours

Sponsors & Collaborators

  • Shahid Beheshti University

    lead OTHER

Principal Investigators

  • Sedighe Mozaffar · Postgraduate student of Shahid Beheshti Medicine University

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
36 Months
Max Age
96 Months
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2010-04-30
Completion
2010-05-31

Countries

  • Iran

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 NCT01118884 on ClinicalTrials.gov