Trials / Unknown
UnknownNCT04239183
BE1 Study Spain - CAPSULE SYSTEM FOR COLOSTOMATES
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 240 (estimated)
- Sponsor
- B. Braun Medical SA · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
A comparative study on the improvement of quality of life of colostomized patients using the new Be1 device with capsule system.
Detailed description
The primary objective is to demonstrate improvement of quality of life (difference of at least 5 points in the StomaQoL questionnaire) among descending colostomy patients, establishing the following comparisons: 1. Patients with recent surgery who after one month using a current two-piece mechanical device switch to the new Be1 device with capsule system versus patients who after one month continue to use the same current two-piece mechanical device during four months. 2. Patients who have been using a current two-piece mechanical device during more than 6 months after an ostomy and agree to switch to the new Be1 device with capsule system during four months. The following secondary objectives have been defined: * Assessment of patient satisfaction with the new Be1 device with capsule system versus a current two-piece mechanical device. * Demonstration that the new Be1 device with capsule system improves the microbiota of the colostomized patient.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Stomatherapy | Demonstrate improvement of quality of life (difference of at least 5 points in the StomaQoL questionnaire (21)) among descending colostomy patients, establishing the following comparisons. |
Timeline
- Start date
- 2020-01-01
- Primary completion
- 2021-01-01
- Completion
- 2021-01-01
- First posted
- 2020-01-23
- Last updated
- 2020-01-23
Source: ClinicalTrials.gov record NCT04239183. Inclusion in this directory is not an endorsement.