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The Effect of Mask Combined With High Flow Oxygen on Preoxygenation During Induction of General Anesthesia in Obese Patients

The Effect of Mask Combined With High Flow Oxygen on Preoxygenation During Induction of General Anesthesia in Obese Patients

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06562660
Enrollment
60
Registered
2024-08-20
Start date
2024-05-01
Completion date
2025-03-01
Last updated
2024-09-20

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

Conditions

Obese

Keywords

High-Flow Nasal Oxygen, Obese Men, Smoking

Brief summary

There is a risk of airway-related incidents during anaesthesia associated with obesity. High-flow nasal oxygen is advocated for perioperative preoxygenation in obese patients to reduce airway adverse reactions. However, there have been no reports on whether smoking behaviors have an impact on obese men's Apnoeic oxygenation with high-flow nasal.This study compared the effects of smoking on the duration of safe apnoea times in obese males.

Detailed description

All patients were were divided into two groups based on smoking status: smokers(S groups), and never smokers(NS groups). Those in the smoking group were current smokers, while those in the nonsmoking group had never smoked. Both groups of patients were induced with intravenous anesthesia and received 5 minutes of high flow nasal oxygen (60 L min) prior to induction.After induction of anaesthesia, the patients were apnoeic until peripheral oxygen saturation decreased to 95 %.

Interventions

DEVICEapnoeic

In group S, High-Flow Nasal Oxygen was performed after the patient lost spontaneous breathing until the end-expiratory oxygen concentration reached 95 %.

Sponsors

Henan Provincial People's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

A total of 60 male obese patients undergoing elective non-thoracic surgery were divided into two groups (n=30) based on smoking status: smokers(S groups), and never smokers(NS groups). Those in the smoking group were current or past smokers, while those in the nonsmoking group had never smoked.

Intervention model description

A total of 60 male obese patients undergoing elective non-thoracic surgery were divided into two groups (n=30) based on smoking status: smokers(S groups), and never smokers(NS groups). Those in the smoking group were current or past smokers, while those in the nonsmoking group had never smoked.

Eligibility

Sex/Gender
MALE
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

1. Participants ranged in age from 18 to 80 with BMI≥30 kg/m2. 2. Participants are male obese patients undergoing elective non-thoracic surgery

Exclusion criteria

: 1. patients were kept awake during the intubation due to cervical spine pathology. 2. Patients with unstable hemodynamics. 3. Patients with airway inflammatory diseases, including asthma, chronic obstructive pulmonary disease (COPD), lung cancer, pulmonary fibrosis and cystic fibrosis. 4. Patients with upper respiratory infection and nasal blockage. 5. Patients with Hypersensitivity to the drug.

Design outcomes

Primary

MeasureTime frameDescription
the safe apnoea times5-minuteInvestigators will record the time of oxygen saturation drop to 95 % during intubation.

Secondary

MeasureTime frameDescription
the Pao2 levels5-minutethe Pao2 levels after 5-minute pre oxygenation with high flow nasal oxygen in two groups of patients.

Countries

China

Contacts

Primary Contacthuabing wang
642221283@qq.com+8618538706687
Backup Contactjiaqiang zhang
Jiaqiang197628@163.com+8613937121360

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 17, 2026