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Exparel pudendal block for Vaginal Prolapse
Phase 4
Waitlist Available
Research Sponsored by Atlantic Health System
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 24 hours before surgery and 72 hours post operative
Awards & highlights
Study Summary
Pudendal Block Using Liposomal Bupivacaine vs. Standard Treatment During Sacrospinous Ligament Fixation
Eligible Conditions
- Vaginal Prolapse
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ daily post-op days 1-3 and 7
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~daily post-op days 1-3 and 7
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pain on postoperative day one
Secondary outcome measures
Ambulatory Quality of Life questionnaire (QoR)
Average pain each day
Most intense pain each day
+6 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Exparel pudendal blockExperimental Treatment1 Intervention
This group will have intra-operative pudendal block performed with Liposomal Bupivacaine (EXPAREL) solution.
Group II: Comparison groupActive Control1 Intervention
This group will be those to receive current standard treatment with no pudendal block performed.
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?
Atlantic Health SystemLead Sponsor
52 Previous Clinical Trials
6,199 Total Patients Enrolled
Frequently Asked Questions
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