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Pelvic floor injection for Postoperative Pain
N/A
Waitlist Available
Research Sponsored by The Cooper Health System
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Able to read English and give informed consent
Undergoing VAGINAL pelvic reconstructive surgery for POP
Timeline
Screening 3 weeks
Treatment Varies
Follow Up postop day #1
Awards & highlights
Study Summary
This trial will test whether injecting painkiller into the pelvic muscles during surgery can reduce post-operative pain for patients with pelvic organ prolapse.
Eligible Conditions
- Postoperative Pain
- Pelvic Floor Prolapse
- Surgery
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ postop day #1
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~postop day #1
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
VAS analog scale on post-op day #1
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Bupivicaine pelvic floor muscle injectionExperimental Treatment1 Intervention
Five injections at pre-specified locations at pelvic floor muscle bilaterally after induction of general anesthesia for vaginal pelvic prolapse surgery
Group II: Standard of care (no injection) preoperativelyActive Control1 Intervention
No injection - standard analgesia
Find a Location
Who is running the clinical trial?
The Cooper Health SystemLead Sponsor
75 Previous Clinical Trials
23,973 Total Patients Enrolled
2 Trials studying Postoperative Pain
310 Patients Enrolled for Postoperative Pain
Frequently Asked Questions
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