N/A
N=22
Analgesic Efficacy of Intravenous Ibuprofen in Biliary Colic
Biliary Colic
Bottom Line
View on ClinicalTrials.gov: NCT02268955 ↗Enrolled (actual)
22
Serious AEs
0.0%
Results posted
May 2019
Primary outcome: Primary: Pain Score 120 Minutes After Study Medication Administration — 3.0; 0.3 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- IV Ibuprofen (Drug); Saline (Drug)
- Age
- Adult · 18+ yrs
- Sex
- All
- Sponsor
- Valleywise Health
- Primary completion
- Jun 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pain Score 120 Minutes After Study Medication Administration |
3.0; 0.3 | — |
Summary
The aim of this study is to assess the analgesic efficacy of intravenous ibuprofen given in the Emergency Department for the treatment of biliary colic. We hypothesize that intravenous ibuprofen will provide a clinically significant drop in self-reported patient pain level as measured by the visual analog scale.
Eligibility Criteria
Inclusion Criteria
- Patients ages 18-55
- Present to ED with right upper quadrant (RUQ) abdominal pain
- Suspected diagnosis of biliary colic
- Negative pregnancy test for women of childbearing potential (complete POC testing form)
- No history of cholecystectomy
Exclusion Criteria
- Patient age 55
- Incarcerated
- Hemodynamic instability
- Inability to reliably self-report or communicate pain intensity and pain relief
- Taking Warfarin
- Cannot consent of are not competent to consent
- Hepatic, renal, cardiac failure
- NSAID or morphine allergy
- History congenital bleeding diathesis or platelet dysfunction
- Peptic ulcer diseases
- Are otherwise unsuitable for the study in the opinion of the investigator/sub-investigators
Data sourced from ClinicalTrials.gov (NCT02268955). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.