Showa Inan General hospital
Komagane, Nagano, 399-4191, Japan
NCT Number: NCT05213208
This study examines that the use of >200 mg of propofol sedation enables patients to drive home safely after outpatient colonoscopy.
Looking for future studies?
Notify Me20 year–90 year
All sexes
Observational
Komagane, Nagano, 399-4191, Japan
The hospital policy of routine discharge to normal activity 1 hour after propofol mono-sedation for EGD or colonoscopy was approved by the ethics committee of Showa Inan General Hospital in January, 2004 (http://www.sihp.jp). The investigator' s subsequent experience verified the safety of this discharge policy which was reconfirmed in March 2014. Based on these studies, the upper limit of 200 mg was established for those allowed early discharge and driving to home.
This study examines that the use of >200 mg of propofol sedation enables patients to drive home safely 90-120 minutes after outpatient colonoscopy.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Using > 200 mg of propofol sedation colonoscopy is performed. 90-120 minutes after colonoscopy subjects go home. Within 1 week patients will be asked about their condition and satisfaction for colonoscopy.
Time frame: 1 day
Number of traffic accidents
Time frame: 1 day
Patient satisfaction (bad, 0-good 100%) is asked.
Showa Inan General Hospital
Other
Propofol Sedation of More Than 200 mg Enables Patients to Drive Home After Outpatient Colonoscopy Including Colorectal Polypectomy
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05142592
Pharmacokinetics, Safety Issues
Portland, Oregon, United States
View Trial DetailsNCT05523596
Safety Issues
Glen Burnie, Maryland, United States
View Trial DetailsNCT05041699
Bleeding, Hemorrhage
Portland, Oregon, United States
View Trial DetailsNCT05518084
Safety Issues
Helsinki, Finland
View Trial Details