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Stimulating Disfunctional Bowel before Ileostomy Closure

Not Applicable
Conditions
Colorectal Neoplasms
C06.405.469.158
Registration Number
RBR-366n64w
Lead Sponsor
Sociedade Beneficente Israelita Brasileira Hospital Albert Einstein
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Adult patients (older than 18 years); with rectal cancer in clinical stages cT3/4Nx or cTxN+; that maybe treated with neoadjuvant chemoradiotherapy; anda submitted to laparoscopic or robotic total mesorectal excision, and submitted to loop protection ileostomy; And also patients who are not undergoing systemic chemotherapy

Exclusion Criteria

Patients who refuse to participate in the study; Patients with a history or suspicion of inflammatory bowel disease; Pregnant patients; Patients who have any contraindication for general anesthesia or surgical intervention

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
It is expected that after ileostomy closure surgery in patients undergoing stimulation of the dysfunctional intestinal loop, there is an improvement in intestinal transit (lower rate of adynamic ileus), verified through clinical reports provided by patients;It is expected that after ileostomy closure surgery in patients undergoing stimulation of the dysfunctional intestinal loop, patients will present a good acceptance of the diet early, that is, it is expected that they will not present symptoms with nausea or vomiting when eating.;It is expected that after ileostomy closure surgery in patients undergoing stimulation of the dysfunctional intestinal loop, patients will have early evacuation, that is, 72 hours after the surgical procedure.
Secondary Outcome Measures
NameTimeMethod
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