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Comparison of oral and buccal midazolam for pediatric dental sedatio

Not Applicable
Conditions
Stress in healthy uncooperative dental patient.
Registration Number
IRCT2013020312350N1
Lead Sponsor
Dental school- Shahed University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
18
Inclusion Criteria

those who needed bilateral and identical restorative and pulp treatment requiring 2 or more dental visits and were unable to tolerate the dental procedure with behavior management techniques. Those with contraindication to Midazolam, upper respiratory tract infection, tonsilar hypertrophy were excluded.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Stress. Timepoint: At discharge. Method of measurement: VAS.;Parents acceptebility. Timepoint: At discharge. Method of measurement: Questionnaire.;Physiologic outcomes. Timepoint: Before treatment,each 10 minutes, at discharge. Method of measurement: Pulse oximeter.
Secondary Outcome Measures
NameTimeMethod
Parental acceptability. Timepoint: Discharge time. Method of measurement: Questionnair.
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