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Observation of nasal high flow oxygen therapy in modified electroconvulsive therapy

Observation of nasal high flow oxygen therapy in modified electroconvulsive therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071678
Enrollment
Unknown
Registered
2023-05-22
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Patients underwent modified electroshock

Interventions

Nasal high flow oxygen therapy group:Transnasal high-flow oxygen therapy
Mask ventilation unit:mask oxygen therapy

Sponsors

First Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Patients who had chosen to receive MECT 2.Patients with ASA grades ? to ? 3.Age 18-60 years old, BMI18 ~ 24kg/m2

Exclusion criteria

Exclusion criteria: 1.Allergic to propofol, succincholine, soy, or eggs 2.Preoperatively predicted difficult airway and upper respiratory tract lesions (tumor, bleeding, infection, etc.) 3.Lung diseases affecting normal oxygenation (pneumonia, COPD, asthma, bronchiectasis, etc.) and other diseases affecting normal ventilation (nasal stenosis, rhinitis, etc.) 4.A person with a clotting disorder

Design outcomes

Primary

MeasureTime frame
Hypoxic-related events during modified electroconvulsive therapy;

Secondary

MeasureTime frame
Modified electroconvulsive therapy indicators;Vital signs during electroconvulsive therapy;Postoperative adverse events;Patient comfort level;Antrum cross-sectional area;Recovery time;Total amount of narcotic drugs;Recovery time of spontaneous respiration;

Countries

China

Contacts

Public ContactZhang Wenjie

First Hospital of Shanxi Medical University

1047479730@qq.com+86 137 0358 6019

Outcome results

None listed

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