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Petrolatum with Non-Stick Gauze for Hidradenitis Suppurativa
N/A
Waitlist Available
Led By Franklin R Blum, BS
Research Sponsored by University of North Carolina, Chapel Hill
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up completed at 1, 2, 4 and 6 weeks post-surgery utilizing images submitted by patients
Awards & highlights
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.
Eligible Conditions
- Hidradenitis Suppurativa
- Surgical Wound
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ collected at 1, 2, 4 and 6 weeks post-surgery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~collected at 1, 2, 4 and 6 weeks post-surgery
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in PUSH Score Over Time
Change in Pain with Dressing Changes
Change in Wound QOL Survey Score Over Time
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Petrolatum with Non-Stick GauzeExperimental Treatment1 Intervention
Participants in this arm will receive petrolatum with non-stick gauze.
Group II: Wet-to-dry DressingsActive Control1 Intervention
Participants in this arm will receive standard of care wet-to-dry dressings.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Petrolatum with Non-Stick Gauze
2022
N/A
~80
Find a Location
Who is running the clinical trial?
University of North Carolina, Chapel HillLead Sponsor
1,519 Previous Clinical Trials
4,195,800 Total Patients Enrolled
2 Trials studying Hidradenitis Suppurativa
47 Patients Enrolled for Hidradenitis Suppurativa
Christopher J Sayed, MDStudy DirectorUniversity of North Carolina, Chapel Hill
1 Previous Clinical Trials
32 Total Patients Enrolled
1 Trials studying Hidradenitis Suppurativa
32 Patients Enrolled for Hidradenitis Suppurativa
Franklin R Blum, BSPrincipal InvestigatorUniversity of North Carolina, Chapel Hill
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- 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.
Research Study Groups:
This trial has the following groups:- Group 1: Petrolatum with Non-Stick Gauze
- Group 2: Wet-to-dry Dressings
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- 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.
Hidradenitis Suppurativa Patient Testimony for trial: Trial Name: NCT05194969 — N/A
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