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Clinical research on unsedated transnasal upper gastrointestinal endoscopy compared with conventional or nitrous oxide sedation endoscopy

Clinical research on unsedated transnasal upper gastrointestinal endoscopy compared with conventional or nitrous oxide sedation endoscopy

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001738
Enrollment
Unknown
Registered
2011-11-29
Start date
2011-10-01
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

diseases of upper digestive tract

Interventions

A:patients undergoing transnasal endoscopy
B:patients undergoing nitrous oxide sedation endosco
C:patients undergoing conventional endoscopy

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 60 years old; 2. Upper GI symptoms, including upper abdominal pain, retrosternal pain, abdominal distension, dysphagia, loss of appetite, and upper GI bleeding; 3. Ability to respond to a self-administered questionnaire, and being nave to transnasal endoscopy.

Exclusion criteria

Exclusion criteria: 1. Allergy to any sedative or anesthetic; 2. Previous history of nasal or abdominal trauma or surgery; 3. Requirement for any possible endoscopic intervention; 4. Pregnancy or lactation; 5. Psychiatric condition and inability to provide informed consent; 6. Uncontrolled hypertension, unstable diabetes mellitus, serious hepatic or renal dysfunction, or cardiopulmonary compromise.

Design outcomes

Primary

MeasureTime frame
duration of in-hospital stay (from reception to discharge);patient satisfaction score;doctor satisfaction score;morbidity/complication rate;pain score;cardiopulmonary variations;nausea/vomiting score;biopsy accuracy;additional medical costs (including agents, consumption);diagnostic spectrum;patient preference;duration of endoscopy (from intubation to withdraw);

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