Clinical Trials Directory

Trials / Unknown

UnknownNCT01121497

The Effect of Physostigmine on Cognitive Functioning in the Immediate Period After Sedation for Colonoscopy

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
160 (estimated)
Sponsor
Rabin Medical Center · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether the administration of physostigmine in combination with sedation for colonoscopy can minimize the cognitive decline at the time of hospital discharge

Detailed description

Physostigmine, a tertiary cholinesterase inhibitor, which prevents the breakdown of ACh by inhibiting the enzyme acetylcholinesterase (AChE), crosses the blood-brain barrier (BBB), and elevates brain ACh levels. Physostigmine has been shown to improve attention, and performance in working memory. It has also been shown to produce analgesia following systemic or central administration. Patients undergoing colonoscopy under sedation of propofol and fentanyl show cognitive decline in the immediate period following the procedure. In this study, half the patients will receive physostigmine in combination with the sedation, and their cognitive functioning at the time of hospital discharge will be assessed by standard neuropsychological tests, and compared to that of patients without physostigmine.

Conditions

Interventions

TypeNameDescription
DRUGPhysostigmineIntravenous bolus of physostigmine 1 mg, 3-5 minutes before completion of the colonoscopy procedure

Timeline

Start date
2010-07-01
Primary completion
2011-07-01
Completion
2011-07-01
First posted
2010-05-12
Last updated
2010-05-12

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01121497. Inclusion in this directory is not an endorsement.