Actively Recruiting
Effect of Synbiotic Supplementation on the Prevention of Mucositis in Cancer Patients Undergoing Chemotherapy
Led by Federal University of Minas Gerais · Updated on 2024-08-29
80
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Introduction: In the 2023-2025 period, colorectal cancer (CRC) will be the third most common type of cancer in Brazil. The most commonly used therapeutic approaches are chemotherapy (QTx) and radiotherapy (RTx). QTx agents, such as capecitabine, affect both malignant cells and normal cells such as gastrointestinal, capillary and immune cells. Cellular damage in the gastrointestinal tract (GIT) results in various symptoms, such as mucositis and diarrhea. Diarrhea is linked to mucosal damage and can result in dehydration, malnutrition and hospitalization, leading to cardiovascular complications and death. Mucositis is inflammation that affects the GIT. This condition makes treatment difficult, leading to reductions, delays or interruption of QTx. These scenarios harm the patient's prognosis and quality of life, resulting in high costs for symptom control, nutritional assistance, management of secondary infections and hospitalization. The Mucositis Study Group (MASCC/ISOO) guidelines recommend the use of probiotics as a preventive measure against diarrhea in cancer patients undergoing QTx and/or RTx. However, the safety of using probiotics in immunosuppressed patients is still controversial and hypotheses are based on epidemiological and experimental studies. This makes it necessary to evaluate whether supplementation with pro- or synbiotics before chemotherapy would have the same beneficial results. Objective: To evaluate the effect of synbiotic supplementation on the prevention, incidence and severity of mucositis in cancer patients undergoing QTx. Method: This is a single-center parallel double-masked randomized clinical trial to be carried out at the Borges da Costa/UFMG Outpatient Clinic at Hospital das Clínicas in Belo Horizonte - Minas Gerais (HC-BH/MG). The inclusion criteria are patients diagnosed with CRC eligible for first-line treatment with Capecitabine, aged ≥ 18 years, both sexes, signed the informed consent form. The study was approved by CEP-UFMG. Expected results: It is expected that supplementation with synbiotics in the pre-QTx period will promote modulation of the microbiota and strengthening of the intestinal barrier, resulting in a lower incidence and severity of mucositis and diarrhea, improving the quality of life of these patients.
CONDITIONS
Official Title
Effect of Synbiotic Supplementation on the Prevention of Mucositis in Cancer Patients Undergoing Chemotherapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with colorectal tumor and starting first oncological treatment
- Age 18 years or older
- Male or female
- Eligible for chemotherapy with capecitabine alone or combined with oxaliplatin
- Patients without colostomy or with colostomy in transverse, descending, or sigmoid colon regions
- Undergoing radiotherapy combined with chemotherapy
- Residing in Belo Horizonte or nearby metropolitan areas
- Signed informed consent form
You will not qualify if you...
- Diagnosis of gastrointestinal carcinoid or stromal tumor (GIST)
- Presence of ileostomy
- Colostomy in the ascending colon
- Inflammatory bowel diseases such as Crohn's disease or colitis
- Use of antibiotics or antifungals within the past 15 days
- Use of prebiotics, probiotics, or synbiotics within the past 15 days
- Use of antidiarrheal medications within the past 15 days
- Presence of fever or mucus discharge
- Pregnant or breastfeeding women
- Patients who refuse to participate in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Escola de Enfermagem - UFMG
Belo Horizonte, Minas Gerais, Brazil, 30130-100
Actively Recruiting
Research Team
S
Simone de Vasconcelos Generoso
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
4
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here