Effect of Synbiotic Supplementation on the Prevention of Mucositis in Cancer Patients Undergoing Chemotherapy: Randomized, Double-masked, Parallel, Single-center Clinical Trial

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Colorectal tumor in the first oncological treatment

• Age over 18 years old

• Both sexes

• Eligible for protocol with capecitabine alone or associated with oxaliplatin

• Patients WITHOUT colostomy or WITH colostomy in the transverse/descending/sigmoid region

• Patient undergoing Radiotherapy treatment associated with Chemotherapy

• Patients residing in Belo Horizonte and the metropolitan region

• Patients who Accept and sign the Informed Consent Form (TCLE)

Locations
Other Locations
Brazil
Escola de Enfermagem - UFMG
RECRUITING
Belo Horizonte
Contact Information
Primary
Simone de Vasconcelos Generoso
simonenutufmg@gmail.com
988128650
Time Frame
Start Date: 2023-12-12
Estimated Completion Date: 2026-12-12
Participants
Target number of participants: 80
Treatments
Placebo_comparator: Capecitabine alone control
n the Control Group, patients received Maltodextrin as supplementation
Experimental: Capecitabine alone synbiotic
In the Intervention Group, patients received the symbiotic Simbioflora as supplementation.
Placebo_comparator: Capecitabine associated with control Oxaliplatin
n the Control Group, patients received Maltodextrin as supplementation
Experimental: Capecitabine associated with synbiotic Oxaliplatin
In the Intervention Group, patients received the symbiotic Simbioflora as supplementation.
Sponsors
Leads: Federal University of Minas Gerais

This content was sourced from clinicaltrials.gov

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