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Clinical Trials/IRCT20221203056700N1
IRCT20221203056700N1
Not yet recruiting
Phase 3

Comparison of the effects of propofol/fentanyl and propofol/apotel for IV sedation during the dental treatment of 2-6 years old precooperative pediatric patients

Shahid Beheshti University of Medical Sciences0 sites38 target enrollmentTBD
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ConditionsAnxiety.Anxiety disorder due to known physiological conditionF06.4

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Anxiety.
Sponsor
Shahid Beheshti University of Medical Sciences
Enrollment
38
Status
Not yet recruiting
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • •2\-6 years old children
  • •Uncooperative
  • •Need to at least two same and symmetric treatment session
  • •ASA 1 health status

Exclusion Criteria

  • •The age under 2 and above 6 years
  • •Cooperative
  • •Lack of similar treatment needs
  • •ASA 2 and more

Outcomes

Primary Outcomes

Not specified

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