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Clinical Trial Summary

This study will be a multicentre randomized controlled trial to assess the efficacy between balloon dilatation and self-expanding metallic stent placement for endoscopic treatment of stenosis in Crohn´s Disease.


Clinical Trial Description

A Prospective, randomized, multicenter clinical trial.

Duration: Beginning in mid-2013 with a minimum of three years depending on the patient inclusion rate.

The participation of at least 20 hospitals in Spain with an inclusion of about 6 patients per hospital is required.

Calculation of sample size: The calculation of sample size was performed considering that the efficacy of endoscopic treatment by endoscopic stent placement is superior to endoscopic dilatation: 75% vs 50% for balloon dilation (% of patients free of therapeutic intervention -endoscopic or surgically a year follow-up).

For all 61 patients are required for each treatment group, the total of 122 patients. This calculation is made taking into account:

- Bilateral Contrast: any two samples may be superior in terms of efficacy.

- Error type I: 0.05

- Error type II: 0.20 (statistical power 80%)

- Percentage of efficacy at one year follow-up: 75% in the prosthetic group and 50% in the balloon dilatation group

- Percentage of losses: 5%.

Schedule

1. Screening Visit

2. Sheet Inclusion

3. Expansion notebook / prosthesis placement notebook

4. Monitoring Worksheet to the 7 days. Symptomatic / complications-incidents assessment.

5. Monitoring Worksheet to the 30 days. Symptomatic / complications-incidents assessment. Includes analytical. In case of placement of prostheses include prosthetic removal sheet

6. Monitoring Worksheet to the 2 months. Symptomatic / complications-incidents assessment.

7. Monitoring Worksheet to the 3 months. Symptomatic / complications-incidents assessment.

8. Monitoring Worksheet to the 4 months. Symptomatic / complications-incidents assessment

9. Monitoring Worksheet to the 5 months. Symptomatic / complications-incidents assessment

10. Monitoring Worksheet to the 6 months. Symptomatic / complications-incidents assessment. Include analytical

11. Monitoring Worksheet to the 7 months. Symptomatic / complications-incidents assessment

12. Monitoring Worksheet to the 8 months. Symptomatic / complications-incidents assessment

13. Monitoring Worksheet to the 9 months. Symptomatic / complications-incidents assessment

14. Monitoring Worksheet to the 10 months. Symptomatic / complications-incidents assessment

15. Monitoring Worksheet to the 11 months. Symptomatic / complications-incidents assessment

16. Monitoring Worksheet to the 12 months. Symptomatic / complications-incidents assessment Include analytical.

17. Final assessment.

18. Monitoring Worksheet to the recurrence. Symptomatic / complications-incidents assessment. Include analytical ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02395354
Study type Interventional
Source Grupo Espanol de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa
Contact Carme Loras, MD
Phone +34-937365050
Email cloras@mutuaterrassa.es
Status Recruiting
Phase N/A
Start date September 2013
Completion date December 31, 2018

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