Clinical Trials Directory

Trials / Completed

CompletedNCT05213208

Safety of Propofol Sedation ( > 200 mg) for Colonoscopy.

Propofol Sedation of More Than 200 mg Enables Patients to Drive Home After Outpatient Colonoscopy Including Colorectal Polypectomy

Status
Completed
Phase
Study type
Observational
Enrollment
300 (actual)
Sponsor
Showa Inan General Hospital · Academic / Other
Sex
All
Age
20 Years – 90 Years
Healthy volunteers
Not accepted

Summary

This study examines that the use of \>200 mg of propofol sedation enables patients to drive home safely after outpatient colonoscopy.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
DRUGPropofolUsing \> 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.

Timeline

Start date
2022-01-16
Primary completion
2024-12-31
Completion
2024-12-31
First posted
2022-01-28
Last updated
2025-05-18

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT05213208. Inclusion in this directory is not an endorsement.