Clinical Trials Directory

Trials / Completed

CompletedNCT01143766

Gabapentin to Improve Patient Tolerance in Endoscopic Retrograde Cholangiopancreatography (ERCP)

Premedication With Single Dose Gabapentin to Improve Patient Tolerance in ERCP: A Double-Blind Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
56 (actual)
Sponsor
Indiana University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The standard approach to sedation in endoscopic retrograde cholangiopancreatography (ERCP) involves the use of benzodiazepines and opiates to achieve a moderate depth of sedation. There is data to suggest supplementing this regimen with gabapentin may lead to reduced pain, higher patient satisfaction and lower opiate requirements. The investigators are conducting a clinical trial to study this hypothesis.

Conditions

Interventions

TypeNameDescription
DRUGGabapentingabapentin 900mg PO x 1 dose, 1 hour prior to the procedure
OTHERStandard sedation regimenCombination opiate and benzodiazepine will be administered to achieve moderate sedation. This is the standard of care.

Timeline

Start date
2010-04-01
Primary completion
2011-12-01
Completion
2011-12-01
First posted
2010-06-14
Last updated
2023-09-28
Results posted
2012-12-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01143766. Inclusion in this directory is not an endorsement.