One Piece Drainable Pouch in Subjects With an Ileostomy

Completed · Phase 2

Conditions studied: Ileostomy

In brief

To assess the safety and performance of an enhanced one piece drainable pouch in subjects with an ileostomy.

Key facts

Study ID

NCT01939106

Run by

ConvaTec Inc.

People needed

12

Starts

2013-06-01

Expected to finish

2013-06-01

Last updated by the study team

2013-09-11

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Of legal consenting age and able to provide written informed consent
• Is able to read, write, and understand the primary language of the investigative site.
• Have an ileostomy for more than 3 months
• 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)
• Have unbroken peri-stomal skin (healthy normal skin to L1 on the SACs Instrument Scale # 1)
• Have a stoma considered 'normal' in appearance in accordance with the stoma, color, moisture and structure rating scales
• Be willing to wear a one piece drainable pouch with moldable wafer according to the usual wear pattern of this type of pouch
• Be willing to participate in the trial for 10 days plus 1 visit prior to the in-residence study period.
• Be willing to remain in residence for 3 days at a central location
• Be willing to meet with the investigator for a total of nine scheduled visits.
• 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
• 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:
• Subjects with a history of sensitivity to any one of the ostomy products or the components being studied
• Subjects with stoma duration of less than 3 months
• Subjects who currently use a belt with their usual appliance
• Subjects who have been entered into the study before, or who have previously taken part in a study in the last month.
• Subjects who require convexity or other skin fillers (pastes, seals, or rings) to even undulations of the peristomal skin
• Subjects undergoing chemotherapy or radiotherapy
• Subjects who have any other medical condition which, according to the investigator justifies exclusion from the study

Where it is running

• Independent Nurse Consultant LLC — Tucson, Arizona, United States

Full record on ClinicalTrials.gov

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