NCT06957444

Rate of Allergic Contact Dermatitis and Cosmetic Outcomes

Enrolling by Invitation
NAAges 18–80InterventionalTreatment
West Virginia University
~600 participants
Updated 2026-05-12 on ClinicalTrials.gov
What's tested:Sylke Adhesive DressingExofin Skin GlueSuture Strip Plus

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Rate of allergic contact dermatitis (4 Days Post Op)
Measured over 4 Days Post-Op
+3 more outcomes measured
Allergic Contact Dermatitis
Osteoarthritis, Hip
Osteoarthritis, Knee
1 sites across 1 states
West Virginia1
  • Benjamin Frye, MD · PRINCIPAL_INVESTIGATOR · West Virginia University Department of Orthopaedics

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

Willing and able to sign the informed consent
Patients presenting to the WVU Medicine Center for Joint Replacement who have a primary TKA or THA surgery scheduled
Patients with surgical wounds closed by 2-0 vicryl and barbed, running v-loc suture (assessed in OR)
Active MyChart account and the ability to take and upload a photo in that system

Exclusion

Patients scheduled for a revision THA or revision TKA
THA used for treatment of a fracture
Patients participating in other studies that might have involve medications such as antibiotics
  • Rate of allergic contact dermatitis (4 Days Post Op)4 Days Post-Op

    Percentage of participants exhibiting allergic contact dermatitis as determined by using the International Contact Dermatitis Research Group (ICDRG) scale with any reaction including and above "Weak Positive" being included in this rate of allergic contact dermatitis: Negative (0): No reaction. Doubtful (+?): Slight erythema (redness) without infiltration. Weak positive (+): Erythema, infiltration, possibly papules. Strong positive (++): Erythema, infiltration, papules, vesicles. Extreme positive (+++): Intense erythema, infiltration, coalescing vesicles, bullous reaction.

  • Rate of allergic contact dermatitis (2 Weeks Post Op)2 Weeks Post-Op

    Percentage of participants exhibiting allergic contact dermatitis as determined by using the International Contact Dermatitis Research Group (ICDRG) scale with any reaction including and above "Weak Positive" being included in this rate of allergic contact dermatitis: Negative (0): No reaction. Doubtful (+?): Slight erythema (redness) without infiltration. Weak positive (+): Erythema, infiltration, possibly papules. Strong positive (++): Erythema, infiltration, papules, vesicles. Extreme positive (+++): Intense erythema, infiltration, coalescing vesicles, bullous reaction.

  • Rate of allergic contact dermatitis (6 Weeks Post Op)6 Weeks Post-Op

    Percentage of participants exhibiting allergic contact dermatitis as determined by using the International Contact Dermatitis Research Group (ICDRG) scale with any reaction including and above "Weak Positive" being included in this rate of allergic contact dermatitis: Negative (0): No reaction. Doubtful (+?): Slight erythema (redness) without infiltration. Weak positive (+): Erythema, infiltration, possibly papules. Strong positive (++): Erythema, infiltration, papules, vesicles. Extreme positive (+++): Intense erythema, infiltration, coalescing vesicles, bullous reaction.

  • Rate of allergic contact dermatitis (3 Months Post Op)3 Months Post-Op

    Percentage of participants exhibiting allergic contact dermatitis as determined by using the International Contact Dermatitis Research Group (ICDRG) scale with any reaction including and above "Weak Positive" being included in this rate of allergic contact dermatitis: Negative (0): No reaction. Doubtful (+?): Slight erythema (redness) without infiltration. Weak positive (+): Erythema, infiltration, possibly papules. Strong positive (++): Erythema, infiltration, papules, vesicles. Extreme positive (+++): Intense erythema, infiltration, coalescing vesicles, bullous reaction.