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95% effective dosage of intranasal dexmedetomidine for sedation in pediatric pulmonary function testing

95% effective dosage of intranasal dexmedetomidine for sedation in pediatric pulmonary function testing

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-17013995
Enrollment
Unknown
Registered
2017-12-16
Start date
2018-01-01
Completion date
Unknown
Last updated
2017-12-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pediatric pulmonary function testing

Interventions

Case series:sedation

Sponsors

Children's Hospital Affiliated Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 3 Years

Inclusion criteria

Inclusion criteria: A total of 70 children were selected for the lung function testing need adequate sedation in children's hospital of chongqing medical university, and the gender was not limited age was 1 ~ 3 years old

Exclusion criteria

Exclusion criteria: children combined with heart failure, pneumonia and hyperthermic

Design outcomes

Primary

MeasureTime frame
MOAA/S score;Aldrete score;

Secondary

MeasureTime frame
heart rate, Spo2;

Countries

China

Contacts

Public ContactTu Shengfen

Children's Hospital Affiliated Chongqing Medical University

519194496@qq.com+86 13983416114

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026