Rectal Cancer Clinical Trial
— FIPIREXOfficial title:
Randomized Clinical Trial of Effects of Synbiotics on Intestinal Microbiota in Patients Undergoing Short-course Preoperative Radiotherapy During Treatment of Rectal Cancer
Verified date | February 2018 |
Source | Region Skane |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of this study is to investigate how bacteria and fibre interact with the epithelial cells of the gastrointestinal mucosa to reduce inflammation and to diminish tissue damage caused by radiation therapy to patients diagnosed with rectal cancer.
Status | Completed |
Enrollment | 30 |
Est. completion date | November 2015 |
Est. primary completion date | November 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Rectal cancer/Adenocarcinoma recti - Informed Consent explained orally and written, understood, agreed and signed Exclusion Criteria: - Diabetes Mellitus - Inflammatory bowel disease - Previous radiation to pelvis area - Ongoing steroid or immunosuppressive therapy - Ongoing antibiotics therapy |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Region Skane |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Action of synbiotics on irradiated GI mucosa in rectal cancer treatment | Reaction of gastrointestinal mucosa in a clinical setting in patients with preoperative radiotherapy treatment of rectal cancer pre-treated with either a probiotic bacteria, blueberry husks and oat bran, oat bran only or no pre-treatment at all, measured by analysis of bacterial diversity. | 2 weeks | |
Primary | Action of synbiotics on irradiated GI mucosa in rectal cancer treatment | Reaction of gastrointestinal mucosa in a clinical setting in patients with preoperative radiotherapy treatment of rectal cancer pre-treated with either a probiotic bacteria, blueberry husks and oat bran, oat bran only or no pre-treatment at all, measured by analysis of inflammation. | 2 weeks |
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