Status:
UNKNOWN
Patient Satisfaction and Safety With Propofol Based Sedation With or Without Fentanyl for Gastrointestinal Endoscopy
Lead Sponsor:
Shandong University
Conditions:
Patient Satisfaction
Eligibility:
All Genders
18-75 years
Phase:
PHASE4
Brief Summary
Patient satisfaction and safety with propofol based sedation with or without fentanyl for gastrointestinal endoscopy
Detailed Description
This study divide patients into two groups, one will be given propofol midazolam and fentanyl; another group was given propofol with midazolam without fentanyl; to observe two groups of patients blood...
Eligibility Criteria
Inclusion
- Patients aged 18 or older
- Patients scheduled for an outpatient gastrointestinal endoscopy by the principal investigator.
Exclusion
- Patients with a history of colorectal surgery
- Patients with ASA class 4 or 5,
- Patients with pre-existing hypoxaemia (SpO2\<90%),
- Patients with hypotension (SBP\<90mmHg)
- Patients with bradycardia (HR\<50 bpm)
- patients with severe chronic renal failure (creatinine clearance\<30 ml/min)
- patients with uncontrolled hypertension (systolic blood pressure\>170 mm Hg, diastolic blood pressure\>100 mm Hg)
- patients with pregnancy or lactation
- Patients hemodynamically unstable
- Patients unable to give informed consent
- Patients with a history of drug allergies;
Key Trial Info
Start Date :
January 1 2019
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
October 30 2019
Estimated Enrollment :
500 Patients enrolled
Trial Details
Trial ID
NCT03803449
Start Date
January 1 2019
End Date
October 30 2019
Last Update
January 14 2019
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