Clinical Trials Directory

Trials / Unknown

UnknownNCT03803449

Patient Satisfaction and Safety With Propofol Based Sedation With or Without Fentanyl for Gastrointestinal Endoscopy

Patient Satisfaction and Safety With Propofol Based Sedation With or Without Fentanyl for Gastrointestinal Endoscopy :a Prospective ,Randomized ,and Cohort Study

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
500 (estimated)
Sponsor
Shandong University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

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 pressure, body movement, and propofol dosage , and the difference in operator satisfaction, and how many people need to give fentanyl again; and two groups of patients after the operation of the reaction, if there are dizziness, nausea, and other adverse reactions; finally, the differences of these two schemes in different populations were analyzed, and the rationalization and individualized medication will be put forward.

Conditions

Interventions

TypeNameDescription
DRUG50-200mg propofolparticipants in both groups are given standard regimen including 50-200mg propofol.
DRUG50ug fentanylparticipants in fentanyl group are given intervention regimen: 50ug fentanyl.
DRUG1 mg midazolamparticipants in both groups are given standard regimen including 1 mg midazolam.

Timeline

Start date
2019-01-01
Primary completion
2019-07-30
Completion
2019-10-30
First posted
2019-01-14
Last updated
2019-01-14

Source: ClinicalTrials.gov record NCT03803449. Inclusion in this directory is not an endorsement.