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

> **NCT03803449** · PHASE4 · UNKNOWN · sponsor: **Shandong University** · enrollment: 500 (estimated)

## Conditions studied

- Patient Satisfaction

## Interventions

- **DRUG:** 50-200mg propofol
- **DRUG:** 50ug fentanyl
- **DRUG:** 1 mg midazolam

## Key facts

- **NCT ID:** NCT03803449
- **Lead sponsor:** Shandong University
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2019-01-01
- **Primary completion:** 2019-07-30
- **Final completion:** 2019-10-30
- **Target enrollment:** 500 (ESTIMATED)
- **Last updated:** 2019-01-14


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03803449

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03803449, "Patient Satisfaction and Safety With Propofol Based Sedation With or Without Fentanyl for Gastrointestinal Endoscopy". Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/clinical/NCT03803449. Licensed CC0.

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