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
| Type | Name | Description |
|---|---|---|
| DRUG | Gabapentin | gabapentin 900mg PO x 1 dose, 1 hour prior to the procedure |
| OTHER | Standard sedation regimen | Combination 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.