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Clinical study on the application of monitoring anesthesia and laryngeal mask anesthesia during awake craniotomy in brain glioma

Clinical study on the application of monitoring anesthesia and laryngeal mask anesthesia during awake cranitomy in brain glioma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17012029
Enrollment
Unknown
Registered
2017-07-18
Start date
2017-08-01
Completion date
Unknown
Last updated
2017-07-24

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

Conditions

brain glioma

Interventions

laryngeal mask anesthesia : laryngeal mask anesthesia
monitoring anesthesia group:monitoring anesthesia without airway protecting

Sponsors

Guangzhou General Hospital of the People's Liberation Army
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged > 18 years, KPS > 60; 2. Clinically and MR imaging, the preliminary diagnosis was brain glioma, and it was proposed to have a clear surgical operation for the removal of glioma; 3. Anesthetic risk assessment American Society of anesthesiology (ASA) I-III; 4. Brain surgery for the first time, and has never received radiation or chemotherapy.

Exclusion criteria

Exclusion criteria: 1. With other malignant tumors, or expected survival less than 3 months; 2. Severe understanding of disability or mental illness may not be able to cooperate with the completion of anesthetic arousal scoring assessment; 3. With other combined diseases, the researchers believe that it may affect the surgical procedure or the effect of anesthesia. 4. Before surgery, ICU should be treated and other anesthetic and sedative drugs may be used. 5. Liver function or renal insufficiency, female pregnancy or lactation; 6. Participating in other studies; 7. The patient refuses to participate and sign the informed consent.

Design outcomes

Primary

MeasureTime frame
Brain tension rating;Narcotrend index scales;VAS pain scores;ICU care duration;

Secondary

MeasureTime frame
Total postoperative consumption of analgesic,in mg,of through 24 hours;the incidence of vomiting and nause in the first 24h after operation;satisfactory degree of doctors;satisfactory degree of patients;

Countries

China

Contacts

Public ContactHe Huan

Guangzhou General Hospital of the People's Liberation Army

hhtgzy@126.com+86 18602019777

Outcome results

None listed

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