Anaesthesia
Conditions
Interventions
propofol group
ketofol group
Sponsors
National liver institute
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: • Adult patients aged 18 to 60 years undergoing ERCP • American Society of Anesthesiologists physical status class I-II.
Exclusion criteria
Exclusion criteria: • Patients with severe cardiovascular disease. • History of bronchial asthma. • Drug allergy to propofol or ketamine. • History of long term uptake of narcotics, benzodiazepine or any neuropsychiatric medication. • Pregnancy. • Obese patient with body mass index more than 36. • History of any neurological insult.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| •Primary aim of the study was to compare propofol and ketofol as a sedative agent regards induction time and recovery time in adult patients undergoing ERCP. | — |
Secondary
| Measure | Time frame |
|---|---|
| • Secondary aim was to investigate the safety and efficacy of both drugs as regards haemodynamic, respiratory compromise, pain, nausea, vomiting, any psychomimetic effect (Agitation, Irritability…) post procedure patient and endoscopiest satisfaction as well as the total dose of drug consumption. | — |
Countries
Egypt
Contacts
Public ContactHESHAM MAGED
MD
Outcome results
None listed