Investigation of a Supporting Ostomy Product Intended for Leakage Detection

Stoma Ileostomy Clinical Trial

Official title:

Investigation of a Supporting Ostomy Product Intended for Leakage Detection

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04894084
• Other study ID #: CP321
• Status: Completed
• Phase: N/A
• Start date: April 29, 2021
• Est. completion date: July 14, 2021

Study information

• Verified date: August 2023
• Source: Coloplast A/S
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

People with intestinal stomas (especially an ileostomy) 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, which has an adhesive sensor layer that should be place underneath the baseplate normally used by the subject. Single arm design. Open-labelled Study duration: 21 days + 3 days.

Description:

Test product is a Digital Leakage Notification System. It consist of a sensor layer (worn beneath the baseplate), a transmitter attached to the sensor layer, a charger for charging of transmitter and an app, to be installed on a smartphone, which notifies the user of the status of their baseplate such as everything looks okay or there is a possible leakage. Subjects are asked to use test product for 21 days. n=15 were using a phone with Android operating system and n=10 a phone with iOS operating system.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: July 14, 2021
• Est. primary completion date: July 14, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Have given written informed consent

2. Be at least 18 years of age and have full legal capacity

3. Have had a stoma for more than three months

4. Have intact skin on the area used in the evaluation meaning no broken skin and only minor discoloration of the skin (assessed by investigator)

5. Be able to use one of the five sensor layer sizes (i.e. Ø40, Ø50, Ø60, Ø70, Ø80 mm)

6. Ileo- or colostomists with liquid output (Bristol scale type 6-7).

7. Currently using a Coloplast product (1pc/2pc Flat/Convex/Concave) from e.g Assura/SenSura/SenSura Mio

8. Have self-reported problems with leakage* (three times within 14 days)

9. Have worry of leakage 'to some, high or very high degree'

10. Is familiar with the use of a smartphone *Leakage: Leakage is defined as output from the stoma on the backside of the baseplate (underneath the baseplate)

Exclusion Criteria:

1. Currently receiving or have within the past 2 month received radio- and/or chemotherapy

2. Currently receiving or have within the past month received topical steroid treatment in the peristomal skin area or systemic steroid (tablet/injection) treatment.

3. Are pregnant or breastfeeding

4. Participating in other interventional clinical investigations or have previously participated in this investigation. Exception: Participation in other Coloplast sponsored clinical investigations is accepted under the circumstances that the subject has paused the activities in the investigation and are otherwise complying with the inclusion and exclusion criteria of this protocol.

5. Known sensitivity towards test product

6. Known sensitivity towards acrylate

7. Is using/have a pacemaker

8. Is using ostomy paste or ostomy powder

Related Conditions & MeSH terms

• Stoma Ileostomy

Intervention

Device:
• CP321
The primary objective is to evaluate the system performance of the test product. This is done by asking subjects to answer questions throughout the study

Locations

Country	Name	City	State
Denmark	Coloplast A/S	Humlebæk

Sponsors (1)

Lead Sponsor	Collaborator
Coloplast A/S

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	System Performance Accuracy of Pictures	The primary endpoint is system performance accuracy: True Negative: No leakage observed on picture and no leakage detected by system; True Positive: Leakage observed in picture and leakage detected by system; False Negative: Leakage observed in picture, but no leakage detected by system; False Positive: No leakage observed in picture, but leakage detected by system	21 days
Secondary	Frequency of Leakage Onto Clothes Before and After Use of Test Product	Subjects are asked to recall numbers of leakage events outside baseplate (and/or onto clothes) the past 3 weeks (at baseline and follow-up). Subjects shall give a specific frequency.	At V1 (baseline) and V2 (follow-up, Day 21)
Secondary	Experience of Leakage Onto Clothes Compared to Only Using Usual Product	Subject own interpretation, Q: to which degree have you experienced leakage onto your clothes with test product?" (5-point scale: very low degree/not at all, low degree, some degree, high degree, very high degree).	V2 (follow-up, Day 21)
Secondary	Reliability of Notifications	Subjects are asked to rate, Q: To which degree did you find notifications from the app reliable and trustworthy (5-point scale; very low degree, low degree, some degree, high degree, very high degree)	V2 (follow-up, Day 21)
Secondary	Ability to Move With Test Product	Q: Compared to your usual product, how was your freedom to move with test product? Much better - better - Same - Worse - Much worse	V2 (follow-up, Day 21)
Secondary	Subjects Worry of Leakage Before and After Use of Test Product	Q: Think back on the last 3 weeks - to which degree have you worried about leakage? Very high degree - High degree - Some degree - Low degree - Very low degree/Not at all	At V1 (baseline) and V2 (follow-up, Day 21)
Secondary	Confidence to Avoid Full Leakage With Test Product Compared to Only Using Usual Product	Q: Compared to your usual product, did you feel confident that you could avoid leakage onto clothes? Yes -No	V2 (follow-up, Day 21)
Secondary	Confidence in Daily Life Compared to Only Using Usual Product	Q: Compared to your usual product, to which degree did the test product give you confidence in daily life? Much higher degree- Higher degree- Same degree - Lower degree- Much lower degree	V2 (follow-up, Day 21)
Secondary	Feeling of Control With Test Product Compared to Only Using Usual Product	Q: Compared to your usual product, did test product give you a feeling of leakage control? Yes, higher leakage control No, lower leakage control	V2 (follow-up, Day 21)
Secondary	Control of Leakage Progression With Test Product Compared to Only Using Usual Product	Q: Compared to your usual product, did the test product give you a feeling of control of leakage progression? Yes, higher control of leakage progression No, lower control of leakage progression	V2 (follow-up, Day 21)
Secondary	Feeling of Security With Test Product Compared to Only Using Usual Product	Q: Compared to your usual product, did you feel more or less secure with test product?	V2 (follow-up, Day 21)
Secondary	Evaluation of Confidence to Increase Social Activities With Test Product Compared to Only Using Usual Product	Q: Compared with your usual product, did the test product affect your confidence to engage in social activities such as seeing friends, and do physical activities? I felt more confident - I felt less confident	V2 (follow-up, Day 21)
Secondary	Evaluation of Sleep With Test Product Compared to Only Using Usual Product	Q: Compared with your usual product, did the test product affect your sleep? Yes, to the better Yes, to the worse No, the same	V2 (follow-up, Day 21)
Secondary	Confidence at Night With Test Product Compared to Only Using Usual Product	Compared with your usual product, to which degree did the test product give you confidence at night? Much higher - Higher - Same - Lower - Much lower	V2 (follow-up, Day 21)
Secondary	Evaluation of Users' Preference	Q: Which product solution do you prefer? Own product - Own product with test product	V2 (follow-up, Day 21)
Secondary	Reason for Preference	Q: What is your reason for preference? (Please tick all that apply); Body fit; Ability to bend and stretch; Feeling of security; Feeling of confidence; Less fear of leakage onto clothes; Discreet to wear; Discreetness in leakage control; Better sleep; Less embarrassment; Other	V2 (follow-up, Day 21)
Secondary	Evaluation of Users' Peace of Mind With Test Product	Q: To which degree did the test product give you peace of mind? Very high degree- High degree- Low degree- Very low degree	V2 (follow-up, Day 21)
Secondary	To Evaluate Users' Assessment of QoL With Test Product Compared to Usual Product	Overall, do you think the test product can improve your feeling of control and confidence to avoid leakage onto clothes and therefore improve your quality of life? Yes - No	V2 (follow-up, Day 21)
Secondary	Adhesive Residue to Skin	To which degree did you experience adhesive residue to the skin in the area around the transmitter? Very low degree/Not at all - Low degree - Some degree - High degree -Very high degree	V2 (follow-up, Day 21)
Secondary	Adhesive Residue to Transmitter	To which degree did you experience adhesive residue on the backside of the transmitter? Very low degree/Not at all - Low degree - Some degree - High degree -Very high degree	V2 (follow-up, Day 21)