WHO ICTRP trial
Assessment of new enhanced ostomy devices in real-life settings in subjects…
NL-OMON44434 · Overview of Medical Research in the Netherlands (NL-OMON) · Not Recruiting
Key facts
| Trial ID | NL-OMON44434 |
|---|---|
| Public title | Assessment of new enhanced ostomy devices in real-life settings in subjects having an ileostomy |
| Scientific title | Assessment of new enhanced ostomy devices in real-life settings in subjects having an ileostomy - CP264 |
| Primary sponsor | Coloplast A/S |
| Registry | Overview of Medical Research in the Netherlands (NL-OMON) |
| Recruitment status | Not Recruiting |
| Study type | Interventional |
| Countries | Denmark;Netherlands |
| Conditions | Artificial opening for faeces; ostomy;10017977;Artificial opening for faeces; ostomy |
| Interventions | After informed consent (V0) has been obtained, there will be a screening visit (V1) lasting up to 6 hours. The study consist of four test periods: Test period 1: Subjects use SenSura Mio® (1-piece/2-piece Open Flat) for 7 + 3 days Test… |
| Registration date | Dec 4, 2017 |
| Target size | 20 |
| Secondary IDs | NL63685.056.17 |
| Registry page | onderzoekmetmensen.nl |
At a glance
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: