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Application of Percutaneous electrical stimulation under fiberoptic bronchoscope for nasal trachea intubation

Application of Percutaneous electrical stimulation under fiberoptic bronchoscope for nasal trachea intubation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17011868
Enrollment
Unknown
Registered
2017-07-05
Start date
2017-08-01
Completion date
Unknown
Last updated
2017-07-10

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

Conditions

Cervical spondylopathy

Interventions

Control group:standard treatment
Percutaneous electrical stimulation group:Percutaneous electrical stimulation

Sponsors

the Third Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: Anterior cervical decompression, bone graft and fusion, internal fixation, Aged >65 years old, American Society of Anesthesiologists(ASA) I to II

Exclusion criteria

Exclusion criteria: High blood pressure, sinus bradycardia, atrioventricular block, hypotension, pulmonary infection, chronic obstructive pulmonary disease and hypoxemia

Design outcomes

Primary

MeasureTime frame
heart rate;systolic pressure;diastolic pressure;Pulse oximetry;BIS;Ramsay;Noradrenaline;—

Countries

China

Contacts

Public ContactQiujun Wang

the Third Hospital of Hebei Medical University

13933178001@163.com+86 18533112929

Outcome results

None listed

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