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Adverse Event Risk Assessment in the Use of Nitrous Oxide for Pediatric Dental Patients

NCT02909816 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 364

Last updated 2018-04-20

No results posted yet for this study

Summary

The objective was to assess adverse event risk in the use of Nitrous Oxide for Pediatric Dental Patients. The investigators performed a multicenter observational study. The investigators included patients aged 1 to 18 years and who have already failed dental care because of non-cooperation; they could be with mental or cognitive disabilities and could have sedative premedication. The investigators performed any type of dental care With the Use of Nitrous Oxide/Oxygen Sedation. The primary outcome was vomiting assessed during or after dental care.

Conditions

  • Dental Carie; Orthodontics

Sponsors & Collaborators

  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Principal Investigators

  • Violaine Smaïl-Faugeron, PhD, DDS · Assistance Publique - Hôpitaux de Paris

Eligibility

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

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2016-09-30
Completion
2018-04-30

Countries

  • France

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 NCT02909816 on ClinicalTrials.gov