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Half effective dose of fospropofol disodium for injection to inhibit responses to laryngeal mask insertion

Half effective dose of fospropofol disodium for injection to inhibit responses to laryngeal mask insertion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106879
Enrollment
Unknown
Registered
2025-07-31
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

None

Interventions

Fospropofol Group:The initial dose of fospropofol disodium for injection in first patient is 10mg/kg, the dose of the next patient is determined by the response to laryngeal mask insertion of the prev

Sponsors

Beijing Shijingshan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. From 18 years old to 65 years old, regardless of gender; 2. Body mass index (BMI) between 18~30 kg/m^2; 3. ASA classification is I-III level; 4. Patients undergoing elective surgery with laryngeal mask general anesthesia; 5. Voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals with contraindications to general anesthesia; 2. Patients with traumatic brain injury, intracranial hypertension, history of cerebrovascular accidents, or central nervous system diseases (such as epilepsy), unstable angina pectoris, myocardial infarction; 3. Patients has obstructive pulmonary disease, respiratory insufficiency, and significant dysfunction of important organs such as the liver and kidneys; 4. History of drug abuse and/or alcohol abuse; 5. Allergy to anesthetic drugs or presence of contraindications; 6. History of mental illness; 7. Disability of communication caused by severe dementia, consciousness disorder, language disorder, etc.

Design outcomes

Primary

MeasureTime frame
ED50 of fospropofol disodium for injection to inhibit responses to laryngeal mask insertion;

Secondary

MeasureTime frame
Blood pressure;Heart rate;SpO2;Anesthesia onset time;Wake time;Adverse drug reaction;

Countries

China

Contacts

Public ContactJie Geng

Beijing Shijingshan Hospital

18401592177@163.com+86 184 0159 2177

Outcome results

None listed

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