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Clinical study for the depth of anesthesia suitable for laryngeal mask placement

Clinical study for the depth of anesthesia suitable for laryngeal mask placement

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019398
Enrollment
Unknown
Registered
2018-11-09
Start date
2018-11-01
Completion date
Unknown
Last updated
2018-11-19

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

Conditions

Patients requiring intravenous general anesthesia

Interventions

Group 1:Propofol
Group 2:dexmedetomidine

Sponsors

Xiamen University Zhongshan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Aged 18 to 60 years old, ASA grade 1 to 2, body mass index 18 to 25 kg/m2.

Exclusion criteria

Exclusion criteria: Severe heart, lung, liver, kidney, and metabolic diseases; arrhythmia; patients who have been taking analgesic or sedative drugs for a long time before surgery; restricted head and neck activity; Mallampati grade III or IV; mouth opening < 2.5 cm; Other clinical trial patients; the researchers believe that other reasons are not suitable for clinical trials

Design outcomes

Primary

MeasureTime frame
BIS;HR;MAP;—

Countries

China

Contacts

Public ContactZhaoxin Zheng

Xiamen University Zhongshan Hospital

zhzhaoxin66@163.com+86 18060995056

Outcome results

None listed

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