Intestinal Failure With a Temporary High-output Double Enterostomy Clinical Trial
— FRYOfficial title:
Impact of Chyme Reinfusion Compared to Parenteral Nutrition on the Incidence of Complications in Patients With a Temporary High-output Double Enterostomy: a Multicentre Randomized Controlled Trial - FRY: efFiciency of Reinfusion of chYme - (FRY)
In the case of intestinal failure with a high-output double enterostomy, the parenteral nutrition (PN) is the gold standard treatment until the surgical reestablishment of digestive continuity. PN has its own morbidity, and in the absence of expertise, the risks of infectious, mechanical, and metabolic complications are increased. Chyme reinfusion (CR) is an enteral nutritional technique which reestablishes the functional continuity of the anatomically present small bowel through an extracorporeal circulation of the chyme. In patients with intestinal failure with a temporary high-output double enterostomy, we hypothesize that CR, compared to PN will reduce post-operative complications after surgical reestablishment of digestive continuity, maintain the intestinal function including absorption, and reduce the complications during the transitional period pending the surgical reestablishment of digestive continuity.
| Status | Not yet recruiting |
| Enrollment | 268 |
| Est. completion date | September 2020 |
| Est. primary completion date | September 2020 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Aged over 18 years - Temporary high-output double enterostomy (=1500ml/24 hours) - Total small bowel length = 120 cm - Downstream small bowel consisting of at least 25 cm of healthy bowel, accessible by a stoma, and suitable for chyme reinfusion - Oral feeding resumed for at least 5 days - Parenteral nutrition or hydration required until the surgical reestablishment of digestive continuity - Affiliation to an health insurance (general Social Security scheme or an equivalent scheme) - No current or planned participation in another biomedical research - Signature of an informed consent form Exclusion Criteria: - Expected duration of parenteral nutrition or chyme reinfusion less than 2 weeks - Refusal by the patient to have a mixed texture diet, - Chemotherapy or radiotherapy before the surgical reestablishment of digestive continuity, - Not drained intra-abdominal collection, - Fever, uncontrolled infection, or infection treated for less than 72 hours, - Shock of any cause, - Creatinine clearance = 60 ml/min - Patients under guardianship. |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| France | Hospices Civils de Lyon - Hôpital de la Croix Rousse | Lyon |
| Lead Sponsor | Collaborator |
|---|---|
| Hospices Civils de Lyon |
France,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | The frequency of complications occurring in patients with a temporary high-output double enterostomy. | The reestablishment of digestive continuity is possible between Month 3 and Month 8 (it is patient-dependent) The complications, and their severity, will be classed using the Dindo-Clavien classification. | From the day which the patient no longer requires surgical care after the surgical placement of a temporary double enterostomy (Day 0) and up to 30 days after the reestablishment of digestive continuity (Month 4 (minus) - Month 9 (plus)) | Yes |