COPPER: A Trial Evaluating Copper-based Products for Incontinence-associated Dermatitis

Hospital Israelita Albert Einstein

Status and phase: Withdrawn; Phase 3; Phase 2

Conditions: Incontinence-associated Dermatitis

Treatments: Combination Product: Barrier product with common diaper; Combination Product: Diaper with a copper-based product + usual care

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT06726707

COPPER_Trial

Details and patient eligibility

About

As there are currently no evidence on the benefit of absorbing incontinence products with copper to stabilize IAD in the elderly, thus, this study will assess the capacity and safety of an absorbing incontinence products with a copper-based substance for the management of adults with incontinence-associated dermatitis, compared to an absorbing incontinence products with no substance. This approach may contribute for IAD management arsenal, since clinical evidence on the efficiency of products available in the market to manage IAD is frail, as seen in systematic reviews mentioned above. We believe copper, as a barrier product, has the potential to perform well in this clinical setting of IAD, as it performed well in other settings.

Full description

This study adopts an exploratory trial design with an adaptive approach. It is randomized, multicenter, controlled, and double-blinded, with parallel groups and blinded outcome adjudication. The study hypothesis suggests that incontinence products infused with copper-based substances may provide superior stabilization of IAD compared to control products.

The primary objective of the study is to evaluate the effectiveness of absorbing incontinence products containing a copper-based substance in stabilizing incontinence-associated dermatitis (IAD) in adults with moderate to severe urinary and/or fecal incontinence. This will be compared against standard absorbing incontinence products without copper-based substances, with both groups receiving usual care. Secondary objectives include assessing improvements in pain within 14 and 28 days, evaluating quality of life improvements over 28 days, and measuring changes in skin health scores from baseline to 14 and 28 days.

Participants will be adults aged 60 years or older, experiencing moderate to severe urinary and/or fecal incontinence. Eligibility will be determined using specific scales outlined in the study rationale. Recruitment will target individuals in long-term care facilities or hospital wards located within São Paulo municipality and its metropolitan area in Brazil. Feasibility assessments will be conducted at each site during an initial visit. Sites deemed suitable will then proceed with participant recruitment.

This study seeks to address critical aspects of managing IAD, particularly through innovative copper-based products. By focusing on clinical endpoints such as pain reduction, quality of life enhancements, and improvements in skin health, the trial aims to provide evidence supporting the potential benefits of copper-infused incontinence products over traditional alternatives.

Sex: All

Ages: 60+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Ability and capability to participate in the study and follow study procedures as determined by the investigator.
• With moderate or more intense urinary (ISI ≥ 3) and/or fecal incontinence (Pescatori et al. (B1, B2, B3, C1, C2, C3);
• Current users of absorbing incontinence products.
• Diagnosed with incontinence-associated dermatitis GLOBIAD 1A or 2A.

Exclusion criteria

• Incontinence-associated dermatitis GLOBIAD 1B or 2B;
• The subject who knows about allergy or a history of an adverse reaction to product ingredients or to any topical preparations or skincare products;
• The subject who has an active skin condition or a history of recurrent skin conditions, except IAD, that may affect IAD healing;
• The subject who was treated in the previous week with systemic or topical agents (except for IAD) that may affect IAD healing process (e.g., steroids);
• Subject with a score < 10 in Mini Nutritional Assessment - Short Form;
• Subjects with diabetes.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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0 participants in 2 patient groups

Copper-based product

Experimental group

Description:

Individuals enrolled in the treatment with diapers embedded with a copper-based product plus usual care

Treatment:

Combination Product: Diaper with a copper-based product + usual care

Control

Active Comparator group

Description:

Individuals enrolled in the treatment with common diapers plus usual care

Treatment:

Combination Product: Barrier product with common diaper