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Comparison of intracranial pressure control by different flow of transnasal oxygen during anesthesia of awake craniotomy

Comparison of intracranial pressure control by different flow of transnasal oxygen during anesthesia of awake craniotomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016621
Enrollment
Unknown
Registered
2018-06-12
Start date
2018-06-18
Completion date
Unknown
Last updated
2018-06-18

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

Conditions

Anesthesia of awake craniotomy

Interventions

Group A:Nasal oxygen flow rate 20L/min
Group B:Nasal oxygen flow rate 40L/min
Group C:Place the tube between epiglottis and vocal cords through nasal cavity

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Patients aged 14-70 years(gender is not limited) 2) planning to receive the elective neurosurgery of awake craniotomy in the brain function area or epilepsy area ; 3) ASA I~II; 4) No aphasia or myodynamia changes were observed before surgery; 5) Informed consent has been signed.

Exclusion criteria

Exclusion criteria: 1. There is a serious system disease and it is in the period of decompensation (such as severe medical complications) : 1) cardiac function = grade 3; 2) respiratory failure; 3) hepatic and renal insufficiency; 4) diseases of the blood system; 5) uncontrolled hypertension; 6) patients with a history of COPD and pulmonary fibrosis, who smoked heavily for a long time before surgery; 7) patients with severe intracranial hypertension and cerebral hernia before surgery; 2. extreme anxiety and fear of surgery, and it is estimated that it is difficult to cooperate in surgery; 3. patients with preoperative consciousness and cognitive dysfunction; 4. preoperative communication disorder, aphasia; 5. patients with pathological obesity (BMI greater than 30) and obstructive sleep apnea syndrome; 6. patients with difficulty to intubation in clinical evaluation; 7. patients with glioma combined with other systemic tumors; 8. female pregnancy; 9. participated in other clinical trials in recent 3 months.

Design outcomes

Primary

MeasureTime frame
Intracranial pressure;PaCO2;PaO2;SpO2;OAA/S score;BIS;

Countries

China

Contacts

Public ContactGU HUAHUA

Huashan Hospital, Fudan University

test@aj.com.cn+86 13918121092

Outcome results

None listed

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