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Clinical Trials/IRCT138804092102N1
IRCT138804092102N1
Completed
Phase 2

A comparison of the sedative effectiveness of oral combinations of midazolam/ketamine and midazolam /hydroxyzine in uncooperative pediatric dental patients

Shiraz university of medical sciences0 sites25 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Dentistry-related anxiety.
Sponsor
Shiraz university of medical sciences
Enrollment
25
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • uncooperative children, ages 37 to 56 months, in need of at least 2 restorative visits, parents acceptance.
  • Exclusion criteria: vomiting before or during treatment.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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