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Petrolatum with Non-Stick Gauze for Hidradenitis Suppurativa
Study Summary
This trial is testing whether wet-to-dry dressings or petrolatum with non-stick bandaging is better for healing after hidradenitis suppurativa (HS) surgery.
- Hidradenitis Suppurativa
- Surgical Wound
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- You cannot participate if you have a preference for a specific type of bandage.You have had trouble using wet-to-dry or petrolatum and non-stick bandages before.You have undergone a standard-of-care surgical procedure for HS with planned secondary intention healing of the wound.
- Group 1: Petrolatum with Non-Stick Gauze
- Group 2: Wet-to-dry Dressings
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Are recruitments currently underway for this clinical experiment?
"According to the information housed on clinicaltrials.gov, this research is currently seeking participants with its initial posting taking place on April 25th 2022 and most recent update occurring two days later."
Is this clinical testing open to participants who are 45 or older?
"This research project is seeking individuals aged 16 and above, but not exceeding 99 years old."
How many participants can be included in this research project?
"Affirmative. According to clinicaltrials.gov, this ongoing medical study is currently accepting participants since its launch on April 25th 2022 and the latest update was just two days later. 80 patients are required from at least one site."
Can I participate in this research endeavor?
"Potential participants in this clinical trial must have a surgical wound and be between 16 to 99 years old. The recruitment goal is approximately 80 individuals."
Who else is applying?
What state do they live in?
What site did they apply to?
What portion of applicants met pre-screening criteria?
How many prior treatments have patients received?
Why did patients apply to this trial?
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