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Local Analgesic

Bupivacaine-Meloxicam for Surgical Incisions

Phase 3
Waitlist Available
Research Sponsored by TriHealth Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
English as first language
Undergoing retropubic mid-urethral sling surgery (with concomitant anterior repair or urethrocele repair)
Must not have
Long acting opioids within 3 days
Any opioids within 24h
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 72 hours post surgery
Awards & highlights

Summary

This trial is testing a combination of two pain-relief drugs applied directly to the surgical site in patients having a specific type of urinary incontinence surgery. The goal is to see if this combination can reduce pain and the need for narcotic painkillers.

Who is the study for?
This trial is for English-speaking patients having retropubic mid-urethral sling surgery, possibly with anterior or urethrocele repair. It's not for those getting additional surgeries like hysterectomy, can't consent, are allergic to the study drugs, pregnant/breastfeeding, recently used steroids or various painkillers.
What is being tested?
The study tests a combined local anesthetic (Bupivacaine-meloxicam) on abdominal incisions in sling surgery patients. It aims to see if this reduces the need for narcotics and lessens pain compared to current practices.
What are the potential side effects?
Potential side effects may include reactions at the injection site such as swelling or itching, possible nerve damage risks associated with injections near nerves, and typical drug-related issues like nausea or headaches.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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English is my first language.
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I am having surgery to support my bladder or urethra.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I haven't taken long-acting opioids in the last 3 days.
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I have not taken any opioids in the last 24 hours.
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I am unable to give consent for my own medical treatment.
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I am having or have had surgery for pelvic organ prolapse or related conditions.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~72 hours post surgery
This trial's timeline: 3 weeks for screening, Varies for treatment, and 72 hours post surgery for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
To determine if use of bupivacaine-meloxicam reduces post-operative narcotic use over the first 3 days following surgery
Secondary study objectives
Compare average pain on each day post operatively
Compare satisfaction with pain control post operatively
Compare worst pain on each day post operatively

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: bupivacaine-meloxicamExperimental Treatment1 Intervention
All patients will receive a total of 20 cc lidocaine with epinephrine injection intra-operatively along the trocar path via the suprapubic incisions, as is standard practice to help with hydrodissection for the procedure. 3-4 cc of bupivacaine-meloxicam will be infiltrated into each suprapubic abdominal incision in the study group
Group II: Standard of CareActive Control1 Intervention
All patients will receive a total of 20 cc lidocaine with epinephrine injection intra-operatively along the trocar path via the suprapubic incisions, as is standard practice to help with hydrodissection for the procedure.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Vulvodynia, such as local anesthetics and NSAIDs, work through different mechanisms to alleviate pain. Local anesthetics like bupivacaine block nerve signals, preventing the transmission of pain to the brain. NSAIDs like meloxicam inhibit COX enzymes, reducing inflammation and associated pain. These treatments are significant for Vulvodynia patients as they address both nerve-related and inflammatory pain, offering a more comprehensive approach to pain management.
[Subarachnoid meloxicam does not inhibit the mechanical hypernociception on carrageenan test in rats].Behavioural assessment of the effects of tumour growth in rats and the influence of the analgesics carprofen and meloxicam.Systemic meloxicam reduces tactile allodynia development after L5 single spinal nerve injury in rats.

Find a Location

Who is running the clinical trial?

TriHealth Inc.Lead Sponsor
98 Previous Clinical Trials
53,615 Total Patients Enrolled

Media Library

Bupivacaine-Meloxicam (Local Analgesic) Clinical Trial Eligibility Overview. Trial Name: NCT05702827 — Phase 3
Stress Incontinence Research Study Groups: bupivacaine-meloxicam, Standard of Care
Stress Incontinence Clinical Trial 2023: Bupivacaine-Meloxicam Highlights & Side Effects. Trial Name: NCT05702827 — Phase 3
Bupivacaine-Meloxicam (Local Analgesic) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05702827 — Phase 3
~49 spots leftby Sep 2025