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Feasibility study on using perfusion index to predict the timing of insertion of laryngeal mask

Feasibility study on using perfusion index to predict the timing of insertion of laryngeal mask

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400083111
Enrollment
Unknown
Registered
2024-04-16
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

Laryngeal mask

Interventions

Case series:No

Sponsors

Children’s Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 13 Years

Inclusion criteria

Inclusion criteria: 1. Short surgery scheduled (surgery time<2 hours) 2. The patient can cooperate with medical staff

Exclusion criteria

Exclusion criteria: 1. Preoperative presence of cardiovascular disease and inability to tolerate non intubated general anesthesia. 2. Emergency department, children with a full stomach. 3. Head and neck as well as oral surgery. 4. Concomitant neurological disorders 5. Receiving treatment with antiepileptic or antidepressant drugs 6. The child does not cooperate and the guardian does not agree

Design outcomes

Primary

MeasureTime frame
perfusion index;perfusion index;perfusion index;—

Secondary

MeasureTime frame
Blood pressure;Heart rate;Respiratory rate;Whether the child moved;Complications(Throat spasm, coughing, bleeding);—

Countries

China

Contacts

Public ContactNi Huanhuan

Children’s Hospital of Nanjing Medical University

Xiaobei7272.student@sina.com+86 137 7057 6224

Outcome results

None listed

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