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NCT06070454 · ClinicalTrials.gov registry record · NA
Prospective Evaluation of Infectious Vulvovaginitis on Wound Complication Rates After Vulvar Excision for Premalignant Lesions
A NA study of Vulvar Diseases and Vaginitis, sponsored by University of Virginia.
- Recruiting
- Registry status
- NA
- Development phase
- 91
- Enrollment target
- 1
- Study location
NCT06070454 is a NA study of Vulvar Diseases and Vaginitis that is actively recruiting participants, run by University of Virginia. The registered enrollment target is 91 participants. The trial reports 1 study location across 1 state.
The verdict
NCT06070454, a NA study of Vulvar Diseases and Vaginitis, is actively recruiting participants, sponsored by University of Virginia.
- RECRUITING
- Registry status
- NA
- Development phase
- 91 participants
- Enrollment target
- 1
- Study location
Study Summary
Primary: * To measure the rate of perioperative vulvovaginitis in a population of patients in central VA with non-malignant vulvar disease who require surgical excision * To correlate the rate of vulvovaginitis with rate of wound cellulitis and incisional breakdown in patients undergoing SPV/WLE for vulvar disease We will use a vulvovaginal swab to test for the most common causes of vulvovaginitis - bacterial vaginosis (BV), trichomonas, and candida. The swab will be collected preoperatively on day of surgery. The outcome will be evaluated by phone call to patient at 1 week after surgery and physical exam at the postoperative visit between 4-6 weeks.
Conditions Studied
Interventions
- DIAGNOSTIC_TEST Vaginitis panel
Study Locations (1)
Virginia
- University of Virginia - Charlottesville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 91 participants |
| Start Date | 2024-04-25 |
| Est. Completion | 2026-08-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06070454
The ClinicalTrials.gov registry entry for NCT06070454 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 91 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Virginia, which has 449 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Vulvar Diseases appearing as the primary indexed condition, and to 1 intervention - of which Vaginitis panel is the first listed.
NCT06070454 reports 1 study location spanning 1 distinct geographic area - top geographies include Virginia.
Frequently Asked Questions
What is clinical trial NCT06070454 about?
NCT06070454 is a clinical study titled "Prospective Evaluation of Infectious Vulvovaginitis on Wound Complication Rates After Vulvar Excision for Premalignant Lesions". Primary: * To measure the rate of perioperative vulvovaginitis in a population of patients in central VA with non-malignant vulvar disease who require surgical excision * To correlate the rate of vulvovaginitis with rate of wound cellulitis and incisional breakdown in patients undergoing SPV/WLE fo...
What is the current status of trial NCT06070454?
This trial is currently recruiting. It is a NA study. The enrollment target is 91 participants. The study started on 2024-04-25. Estimated completion is 2026-08-01.
What conditions does trial NCT06070454 study?
This clinical trial studies the following conditions: Vulvar Diseases, Vaginitis.
What interventions are being tested in trial NCT06070454?
The interventions under investigation include: Vaginitis panel (DIAGNOSTIC_TEST).
Who is sponsoring clinical trial NCT06070454?
This trial is sponsored by University of Virginia, which has 449 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06070454 being conducted?
This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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