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Clinical Trial Summary

This is an open-labelled randomized cross-over and controlled exploratory intervention that aims to include 20-30 patients with an ileostomy. Every patient is to test two new ostomy appliances each for two weeks. During the test a questionaire is to be filled out and interviews will take place. Primary parameter is leakage. A Study nurse will visit the participants in their homes every two week during the test.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT01523756
Study type Interventional
Source Coloplast A/S
Contact
Status Completed
Phase N/A
Start date February 2012
Completion date April 2012

See also
  Status Clinical Trial Phase
Terminated NCT01517178 - Multi-national, Safety and Performance Study of New Ostomy Product Compared to Standard Care Phase 3
Withdrawn NCT01448629 - Safety and Performance of a New 1-piece Ostomy Product Compared to Standard Care Ostomy Products in Subjects Ileostomy N/A
Not yet recruiting NCT06310070 - 3D Printed Personalized Ostomy Appliance N/A
Completed NCT01784458 - Clinical Significance of Intra-abdominal Hypertension in Surgical Patients With Severe Sepsis N/A
Completed NCT05147870 - Outcome After Laparoscopic Surgery for Peptic Ulcer Perforation