Investigation of Heylo, a Novel App Driven Digital Supporting Ostomy Product
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About
People with intestinal stomas can have, despite development of better ostomy products, problems with leakage which influence their quality of life negatively.
To overcome this, Coloplast has developed a new supporting ostomy product called Heylo™, which has an adhesive sensor layer that should be placed underneath the baseplate. The sensor layer consists of an electronic sensor system that continuously detects moisture and output leakage underneath the baseplate. A transmitter connected to the sensor layer continuously evaluates the incoming information and sends a status to a smartphone software application, which based on a predefined flow decides which information to deliver to the user about the baseplate status.
The overall aim of this clinical investigation is to evaluate the benefits of the new supporting product, Heylo compared to Standard of Care.
Full description
The Investigational device - Heylo, is already CE-marked.
The investigation is an open-labelled, randomized cross-over trial with two test periods evaluating Heylo and Standard of Care.
In total 144 subjects having an ileostomy or an colostomy will be included and randomized.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Has given written consent to participate by signing the Informed Consent Signature Form.
- Is at least 18 years of age and has full legal capacity.
- Has an ileostomy or colostomy with consistent liquid/mushy fecal output (5-7 Bristol scale*)
- Is able to use one of the five test products (i.e. Ø40, Ø50, Ø60, Ø70, Ø80 mm).
- Has experienced leakage** under the baseplate at least three times within the last fourteen days. **Leakage defined as output seeping under the baseplate"
- Has worry about leakage to "some degree, high degree, or very high degree" (on a five-point Likert scale: Very low degree/Not at all, Low degree, some degree, High degree, very high degree)
- Is willing to refrain from use of ostomy paste.
- Has a smartphone compatible with the Heylo™ application
- Is able to follow study procedures for 4 months (assessed by investigator or delegate)
Exclusion criteria
- Is participating in other clinical investigations or has previously participated in this investigation
- Is pregnant or breastfeeding
- Has known hypersensitivity towards any of the products used in the investigation
- Is using/ has a pacemaker
Trial design
Primary purpose
Allocation
Interventional model
Masking
144 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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