Status:
COMPLETED
Optimization of Sedation Protocol for Endoscopic Procedures Using Impedance Ventilation Monitor.
Lead Sponsor:
Charles University, Czech Republic
Collaborating Sponsors:
Military University Hospital, Prague
Conditions:
Sedation Complication
Ventilatory Depression
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
The aim of the study is to evaluate the effect of opioids administered during sedation on patients' respiratory activity (ventilation) and comfort of the operator and patient during the endoscopic pro...
Detailed Description
The aim of the study is to evaluate the effect of opioids administered during sedation on patients' respiratory activity (ventilation) and comfort of the operator and patient during the endoscopic pro...
Eligibility Criteria
Inclusion
- Scheduled therapeutic or diagnostic colonoscopy with sedation
- Supine or lateral decubitus position
- Age 18-65
- American Society of Anesthesiologists (ASA) physical status classification system 1-2
- Informed consent signed
Exclusion
- Planned frequent use of electrocoagulation
- Contact allergy for adhesive pads, excessive thoracic hair or other problem with pads
- contraindication of using Propofol or Fentanyl
- Incapability to understand the informed consent
Key Trial Info
Start Date :
November 16 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 22 2025
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT06060626
Start Date
November 16 2023
End Date
January 22 2025
Last Update
January 28 2025
Active Locations (1)
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1
Military University Hospital Prague
Prague, Czechia, Czechia, 16209