A clinical trial investigating the effect of Lanreotide on reducing fistula output in patients with high output enterocutaneous fistula

Update Il y a 4 ans
Reference: EUCTR2013-003998-10

Woman and Man

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Extract

To assess the impact of treatment with Lanreotide versus current standard of treatment on output reduction in patients with high output enterocutaneous fistulas or enterostomies.


Inclusion criteria

  • All adult patients with a small bowel fistula with an output > 500ml/day or a an enterostomy with an output > 1500ml/day after gastro-intestinal, abdominal wall surgery. Randomization is possible if patients are at least 4 weeks postoperative and had at least 2 weeks of standard care (loperamide, codeine, PPI)

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