A Randomized Clinical Study Comparing Two Closure Techniques of Excised Keloids

University of Miami

Status

Terminated

Conditions

Keloid

Treatments

Device: Clozex

Procedure: Suture

Study type

Interventional

Funder types

Other

Identifiers

NCT00519493

20061027

Details and patient eligibility

About

This investigator initiated study, single-blinded, parallel, randomized study will be conducted in subjects with 2 or more keloids similar in size and duration on a similar area of the body. The response of the closure techniques will be evaluated by clinical and instrumental assessments. Each qualified subject will be assessed and the keloids will be randomly assigned to the Clozex or suture closure. One keloid will be surgically excised and the surgical wound generated will be randomized to be closed with Clozex. A second keloid will be surgically excised and the surgical wound generated will be randomized to be closed with sutures. The inflammation index and the keloid recurrence rate at each surgical wound closure site will be compared.

Full description

This study will be undertaken to compare the efficacy of two closure techniques for excised keloids. (1) Clozex, a non-latex, hypoallergenic adhesive polymeric interlaced film designed to adhere to proximal wound edges for 7-10 days, will be used after the punch biopsy or excision of a keloid and (2) sutures to close a similar second keloid after the punch biopsy or excision of a keloid.

On day 12, the investigator and subject will assess the keloid site(s) with the use of a visual analog scale.

There is an optional follow-up at 3 months and 6 months to assess the recurrence of the keloid and the effectiveness of the treatments with a visual analog scale.

The subject will assess the keloid site(s) with the use of the following visual analog scale:

Cosmetic appearance
Pain
Tenderness
Itching
Oozing
Redness
Warmth

The investigator will assess the keloid site(s) with the use of this visual analog scale:

Global appearance
Color
Matte/Shiny
Contour
Distortion
Texture
Oozing
Redness
Warmth
Firmness

Enrollment

3 patients

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male or females, in good health, and at least 12 years of age.
Individuals with 2 or more keloids on the trunk, arm, leg, and neck between 0.5 and 2 cm in length.
Individuals who are willing and able to participate in the requirements of the study, including signing the informed consent.
In the opinion of the investigator, the 2 keloids can be excised in a similar manner and closed properly with the two techniques and will benefit from the procedure.
In the opinion of the investigator, the keloid could benefit from surgical procedure.

Exclusion criteria

Individuals with keloids that do not fit into the criteria.
Individuals who are planning pregnancy, pregnant, or breast feeding.
Individuals with a history of medical or dermatologic conditions which, in the opinion of the investigator, would put the subject at heightened risk or would limit complicate the study evaluations required by the protocol.
Individuals who present with excessive body hair in the designed keloid area.
Individuals with uncontrolled diabetes.
Individuals with autoimmune disorders (HIV/AIDs, SLE).
Subjects who have received keloid treatment within one month of the first day of the study.
Individuals who plan to receive keloid treatment(s) during the study.
Individuals who are currently taking prescription or over the counter medication or interventions on a regular basis that as part of their mechanism of action, have the potential to mask an inflammatory reaction. Examples of such medications include, but are not limited to, corticosteroids, non-steroid anti-inflammatory drugs (NSAIDs), antihistamines, aspirin (81mg or less daily dosage permissible), or other medications that in the opinion of the investigator or designee may expose the subject to heightened risk or complicate the study assessments.