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Evaluation of End-tidal CO2 Measurement Via Nose and Pharynges in Non-intubated Patients During Digital Subtraction Cerebral Angiography

Evaluation of End-tidal CO2 Measurement Via Nose and Pharynges in Non-intubated Patients During Digital Subtraction Cerebral Angiography

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONRC-11001414
Enrollment
Unknown
Registered
2011-07-01
Start date
2011-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Patients treated by Digital Subtraction Cerebral Angiography

Interventions

1:Nil

Sponsors

Department of Anesthesiology, West China hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Male and female aged 18 to 65 years old; 2. Unconscious, ASA physical status I-III patients; 3. Undergoing digital subtraction cerebral angiograph

Exclusion criteria

Exclusion criteria: Patients with severe pulmonary disease (pulmonary tuberculosis, pulmonary interstitial fibrosis, chronic obstructive pulmonary disease) were excluded. Patients with shunt disease, fever, or who have high risk for aspiration such as reflux esophagitis, severe intracranial hypertension, and nausea and vomiting frequently were also excluded.

Design outcomes

Primary

MeasureTime frame
PETCO2';PaCO2;PETCO;

Countries

China

Contacts

Public ContactRurong Wang
rr1wang@yahoo.cn+86 18980601563

Outcome results

None listed

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