Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06576986

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Escola de Enfermagem - UFMG

Belo Horizonte, Minas Gerais, Brazil, 30130-100

Actively Recruiting

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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

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