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A Single-center, randomized, opening clinical studies about nasopharyngeal airway used in obesity patients who undergo painless gastroscopy

A Single-center, randomized, opening clinical studies about nasopharyngeal airway used in obesity patients who undergo painless gastroscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPR-15006216
Enrollment
Unknown
Registered
2015-04-08
Start date
2015-04-10
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

diseases of upper digestive tract

Interventions

Group A :use nasopharyngeal airway
Group B:not use nasopharyngeal airway

Sponsors

Daping Hospital, the Third Military Medical University, Chongqing, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) patients proposed painless gastroscopy of age 18-70 years, male or female; (2) BMI greater than 28kg/m2; (3) American Society of Anesthesiologists (ASA) classification as Class I-III; (4) correctly answered the questionnaire; (5) signed informed consent.

Exclusion criteria

Exclusion criteria: (1) nasal polyps, bleeding tendency, nasal trauma, nasal deformity, nasal inflammation; (2) a serious heart, lung, liver, kidney and metabolic disorders, electrolyte imbalance; (3) blood pressure >180/90mmHg; (4) ECG prompt block or complete left bundle branch II degree atrioventricular block;

Design outcomes

Primary

MeasureTime frame
Oximetry;

Secondary

MeasureTime frame
Operation time;Recovery time;heart rate;Blood pressure;first aid treatment;Adverse Events;Satisfaction;

Countries

China

Contacts

Public ContactChunhui LAN
tiandaochouqin99@hotmail.com+86 13896067955

Outcome results

None listed

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