Trials / Terminated
TerminatedNCT02618668
Haemodynamic Stability of Ketamine/Propofol Admixture "Ketofol" in Patient Undergoing Endoscopic Retrograde Cholangio Pancreatography
Haemodynamic Stability of Ketamine / Propofol Admixture "Ketofol" in Patient Undergoing Endoscopic Retrograde Cholangio Pancreatography
- Status
- Terminated
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 90 (actual)
- Sponsor
- Assiut University · Academic / Other
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
The investigators aim to evaluate the effect of Ketamine/Propofol Admixture on hemodynamic stability, recovery time ,patient \& doctor satisfaction scores during Endoscopic Retrograde Cholangiopancreatography.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ketamine / Propofol Admixture | propofol-ketamine 3:1 mixture(%1 15 ml propofol + 1 ml 50mg/ml ketamine+4 ml saline in a 20-ml syringe which resulted in0.25 mg.ml-1 ketamine and 0.75 mg.ml-1 propofol |
| DRUG | Propofol | 2 mg/kg I.V |
Timeline
- Start date
- 2015-07-01
- Primary completion
- 2018-07-01
- Completion
- 2018-09-01
- First posted
- 2015-12-01
- Last updated
- 2019-09-23
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT02618668. Inclusion in this directory is not an endorsement.