Intraoperative Wound Irrigation for Pilonidal Disease
Part of paid clinical trials in Palo Alto, California.
- Sponsor
- Stanford University
- Study ID
- NCT07417202
- Status
- Recruiting
Conditions
- Pilonidal Disease
Eligibility Criteria
- Sex
- ALL
- Age
- 8 Months - 30 Years
- Healthy Volunteers
- Not accepted
Interventions
- Hypochlorous Acid — PROCEDUREHypochlorous acid will be used as the wound irrigation solution instead of the saline which is currently considered standard. All other aspects of the surgery will be the same across both arms.
Study Details
The purpose of this study is to determine the best method for cleaning wounds during surgery for patients with Stage 3 pilonidal disease. The investigators will compare the standard wound cleaning solution, saline, with a different solution called hypochlorous acid (Vashe, Urgo Medical) to see which one helps wounds heal faster after surgery.
Key Dates
- Start date
- Mar 1, 2026
- Status verified
- May 2026
- Primary completion
- Sep 30, 2028
- Completion
- Feb 28, 2029
Study Design
- Enrollment
- 72 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: VasheParticipants in this arm will have a hypochlorous acid solution used for wound irrigation intraoperatively.
- No Intervention: SalineParticipants randomized to this arm will have a saline solution used for wound irrigation, which is the current standard of care.
Primary Outcome Measure
Time to Wound Closure [ Time Frame: From day of surgery to wound closure at ~14 days ]
Central Contacts
- Elena Harnish, MA650-739-6427
- Elton Ortiz, MS650-723-6439
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Lucile Packard Children's Hospital - Stanford | Palo Alto | California | 94304 | Bill Chiu, MD (PRINCIPAL_INVESTIGATOR) |
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