Home › NCT07417202
Intraoperative Wound Irrigation for Pilonidal Disease
Recruiting
Intraoperative Wound Irrigation for Pilonidal Disease: A Randomized Controlled Trial
Who can join
8 Months – 30 Years · All sexes
Full eligibility criteria
Inclusion Criteria: * Stage 3 pilonidal disease according to the Stanford Pilonidal Severity Staging System Exclusion Criteria: * Patients with pilonidal disease that is not classified as stage 3 * Intellectual disability precluding the patient and/or guardian from being able to consent
About the study
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.
What is being tested
- Hypochlorous Acid (procedure)
Sponsor: Stanford University · Participants: 72 · Started: Mar 1, 2026
Contact the study team
- Elena Harnish, MA · Phone: 650-739-6427
- Elton Ortiz, MS · Phone: 650-723-6439
Official record on ClinicalTrials.gov — NCT07417202
Locations in the U.S.
| California | Lucile Packard Children's Hospital - Stanford, Palo Alto |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.