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
| Type | Name | Description |
|---|---|---|
| DRUG | 50-200mg propofol | participants in both groups are given standard regimen including 50-200mg propofol. |
| DRUG | 50ug fentanyl | participants in fentanyl group are given intervention regimen: 50ug fentanyl. |
| DRUG | 1 mg midazolam | participants 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.