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Exparel for Urinary Tract Infection
Phase 4
Waitlist Available
Research Sponsored by Loma Linda University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients undergoing urologic surgery.
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 days postoperatively
Awards & highlights
Study Summary
This trial looks at whether a new painkiller is effective for people undergoing urologic surgeries.
Eligible Conditions
- Urinary Tract Infection
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 30 days postoperatively
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 days postoperatively
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Length of Hospital Stay and readmission
Postoperative complications
Postoperative pain assessment
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: ExparelExperimental Treatment1 Intervention
This arm will receive intraoperative local Liposomal Bupivacaine injection (Exparel) at the port placement site.
Group II: MarcaineActive Control1 Intervention
This group will receive will local bupivacaine HCl (Marcaine) injection at the port placement site.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Bupivacaine
FDA approved
Find a Location
Who is running the clinical trial?
Loma Linda UniversityLead Sponsor
306 Previous Clinical Trials
260,848 Total Patients Enrolled
Mohamed Keheila, MDStudy DirectorLoma Linda University Medical Center
2 Previous Clinical Trials
15 Total Patients Enrolled
Frequently Asked Questions
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