Using EMLA cream to improve comfort during outpatient scrotal surgeries
Official title: Efficacy of EMLA Cream Assisted Loco-sedation for Office-based Andrology Procedure: A Randomized Controlled Study
Run by University of Manitoba · NCT06242977 · Data updated 2026-05-14
This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.
This study tests if using EMLA cream can make outpatient scrotal surgeries more comfortable for patients compared to just using local anesthesia alone.
Quick facts
| Phase | Phase 3 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years to 65 Years |
| Sex | Men only |
| Enrollment | 72 (estimated) |
| Sponsor | University of Manitoba Academic / other |
| Locations | 1 site (Winnipeg, Manitoba) |
| Trial ID | NCT06242977 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adult patients scheduled for specific scrotal surgeries under local anesthesia.
✕Probably not a fit
Patients who require sedation or do not consent to randomization will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial investigates the effectiveness of EMLA cream, a topical anesthetic, in enhancing patient comfort during office-based scrotal surgeries performed under local anesthesia. The study compares the experiences of patients receiving local anesthesia alone to those receiving local anesthesia with EMLA cream. By moving these procedures from hospital settings to outpatient clinics, the trial aims to demonstrate the benefits of reduced complications, lower costs, and improved patient satisfaction. The goal is to determine if EMLA can further increase tolerability and reduce anxiety associated with these procedures.
Why it matters
Potential benefit: If successful, this approach could significantly improve patient comfort and satisfaction during outpatient scrotal surgeries.
How similar studies have gone: Previous studies have shown positive outcomes with EMLA cream in other urologic procedures, suggesting potential for success in this context.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patients undergoing hydrocelectomy, spermatocelectomy, epididymectomy, testicular biopsy, scrotal lesion or cyst excision under local anesthesia alone were included. Exclusion Criteria: * Patients were excluded if their procedure was to be performed with sedatives (e.g., inhaled nitrous oxide gas, oral, or IV sedation) or did not provide consent to be randomized
Where it's running
-
Men's Health Clinic Manitoba
Winnipeg, Manitoba, Canada Recruiting
Study contacts
- Study coordinator: Premal Patel, MD
- Email: ppatel5@hsc.mb.ca
- Phone: 204-221-4476
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.