Safety and Performance of Flexima®/Softima® Stoma Appliances in Enterostomy Patients

Stoma Ileostomy Clinical Trial

Official title: Prospective, Non-interventional, Post-Market Clinical Follow-up Investigation of the Safety and Performance of Flexima®/Softima® Stoma Appliances in Enterostomy Patients

Status Recruiting

Clinical Trial Summary

The study is designed as a non-interventional, prospective, international, multi-center, post market follow-up investigation. The product under investigation will be used in routine clinical practice and according to Instructions for Use (IFU). The data obtained during routine clinical use will be documented in electronic Case Report Forms (eCRF).

The investigation will consist of an enrolment visit (Visit 1, or V1) and a final visit (Visit 2, or V2). The duration between the two visits is 14 (±3) days.

Clinical Trial Description

Details of the procedures performed at each visit follow.

#A ENROLMENT VISIT (Visit 1, onsite)

The following procedures will be performed:

• Informed consent

• Eligibility assessment

• Record demographics

• Record medical and surgical history (including stoma details)

• Record details of the appliance currently used, which could be different than a Flexima®/Softima®. However, participation in the investigation requires a Flexima®/Softima® appliance be used.

• Peristomal skin assessment (DET scoring)

• Discuss investigation requirements with the participant, including the need of adequately completing the patient's diary

• Start recording adverse events and concomitant medications

• B 14 (±3 DAY) DEVICE WEARING TIME (telephone follow-up)

During the wearing time, the following procedures will be done:

• The clinical site personnel will follow-up with the participants by telephone as required

• Participants will complete the patient's diary, which includes a record of appliance changes and assessment of leakages

• Record adverse events and concomitant medications (via telephone follow-up)

• C FINAL VISIT (Visit 2, onsite)

During the final visit, the following procedures will be done:

• Peristomal skin assessment (DET scoring)

• Participant evaluation of device performance (see 8.2.7)

• The responsible site personnel will review the patient's diary together with the patient. Any missing data will be discussed with the patient and, if possible, completed. In case it can't be completed, clarification notes explaining the reason for the missing data are to be added to the patient's diary (e.g. details forgotten)

• Record adverse events and concomitant medications ;

Related Conditions & MeSH terms

• Enterostomy
• Stoma Colostomy
• Stoma Ileostomy

• NCT number: NCT05373888
• Study type: Observational
• Source: BBraun Medical SAS
• Status: Recruiting
• Start date: April 1, 2022
• Completion date: March 31, 2023