Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 2:43 PM
Ignite Modification Date:
2025-12-26 @ 2:43 PM
NCT ID:
NCT01939106
Eligibility Criteria:
Inclusion Criteria
1. Of legal consenting age and able to provide written informed consent
2. Is able to read, write, and understand the primary language of the investigative site.
3. Have an ileostomy for more than 3 months
4. Currently a one or two piece drainable pouch user (all attempts will be made to include ConvaTec Active Life or Esteem Plus one piece closed pouch users)
5. Have unbroken peri-stomal skin (healthy normal skin to L1 on the SACs Instrument Scale # 1)
6. Have a stoma considered 'normal' in appearance in accordance with the stoma, color, moisture and structure rating scales
7. Be willing to wear a one piece drainable pouch with moldable wafer according to the usual wear pattern of this type of pouch
8. Be willing to participate in the trial for 10 days plus 1 visit prior to the in-residence study period.
9. Be willing to remain in residence for 3 days at a central location
10. Be willing to meet with the investigator for a total of nine scheduled visits.
11. Be willing to discontinue the use of pastes, adhesive strips and rings/seals used to seal the area between the skin barrier wafer and stoma during the use of the study device
12. Other than their ileostomy considered to have a healthy/stable health status Have good manual dexterity and be able to take care of their stoma independently Be willing and able to complete a diary card for the duration of the study. Be willing to take photographs of the stoma and pouch on pouch removal
Exclusion Criteria - The following subjects must not be included into the study:
1. Subjects with a history of sensitivity to any one of the ostomy products or the components being studied
2. Subjects with stoma duration of less than 3 months
3. Subjects who currently use a belt with their usual appliance
4. Subjects who have been entered into the study before, or who have previously taken part in a study in the last month.
5. Subjects who require convexity or other skin fillers (pastes, seals, or rings) to even undulations of the peristomal skin
6. Subjects undergoing chemotherapy or radiotherapy
7. Subjects who have any other medical condition which, according to the investigator justifies exclusion from the study
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01939106
Study Brief:
Protocol Section:
NCT01939106