FindTrial
Sign In

Sedation-related adverse events during gastrointestinal endoscopy: a prospective, observational cohort study

Sedation-related adverse events during gastrointestinal endoscopy: a prospective, observational cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300078784
Enrollment
Unknown
Registered
2023-12-18
Start date
2023-12-19
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Gastrointestinal endoscopy

Interventions

Observation group:N/A

Sponsors

The First Affiliated Hospital of Naval Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Patients who will be sedated for gastrointestinal endoscopy, 2. Age = 18 years

Exclusion criteria

Exclusion criteria: 1.Patients who are unable to cooperate in completing information collection prior to sedation, 2.Patients scheduled for general anaesthesia with endotracheal intubation, 3.Patients for whom the investigator's safety concerns preclude sedation.

Design outcomes

Primary

MeasureTime frame
Hypoxemia;Hypotension;Bradycardia;Reflux and aspiration;Unplanned hospitalization;Endotracheal intubation;CPR or death;—

Secondary

MeasureTime frame
Hypertensive;Tachycardia;Nausea and vomiting;Laryngeal spasm;Falling off the bed;—

Countries

China

Contacts

Public ContactLulong Bo

The First Affiliated Hospital of Naval Medical University

bartbo@smmu.edu.cn+86 138 1728 3189

Outcome results

None listed

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