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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06199752
Other study ID # Synbiotics in cancer
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date December 12, 2021
Est. completion date September 10, 2023

Study information

Verified date December 2023
Source Theodor Bilharz Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this interventional study was to evaluate the synergistic effect of symbiotics (a combination of probiotics and prebiotics) compared to probiotics alone in terms of their impact on anti-tumor immunomodulation in patients with pancreatic ductal adenocarcinoma (PDAC). The study also aimed to assess the effects of these interventions on postoperative complications and outcomes. In the study, a probiotic agent (Nowfoods, USA), containing ten strains of bacteria with a total dosage of 25 billion colony-forming units (CFU) was administered. This probiotic regimen involved taking two capsules once daily, starting two weeks before the surgery and continuing for one month after the surgery. For the synbiotic group, in addition to the probiotic agent, two capsules per day of inulin supplement (HERBAMAMA, USA) were also taken. The study included three groups: the synbiotics group, the probiotics group, and the placebo group. The researchers compared the pathological status of immune cell infiltration (specifically CD8 cells) and interferon-gamma expression, as well as the levels of interleukins 10, 6, and 10 in the participants' serum. Four blood samples were collected from each participant: one taken 14 days before the surgery, one on the surgery date, one two weeks after the surgery, and one 30 days after the surgery. The main research question addressed by the study was whether there was a significant difference in the immunomodulatory effect and postoperative complications between the synbiotics group and the probiotics group. The placebo group likely served as a control to compare the effects of the interventions against no intervention.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date September 10, 2023
Est. primary completion date April 20, 2023
Accepts healthy volunteers No
Gender All
Age group 25 Years to 65 Years
Eligibility Inclusion Criteria: - Patients with primary PDAC with complete pathological and follow-up data - Patients without long-distance metastasis - Patients without chronic diseases - Patients without any treatments before the surgery. Exclusion Criteria: - Patients who suffered from other tumors or other chronic diseases or accidentally died - Lack of pathological and follow-up data. - Patients with long-distance metastasis before the surgery.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
probiotic agent 25 Billion CFU (Nowfoods, USA) , ). Inulin capsules 1000mg Herbamama USA
probiotic agent 25 Billion CFU (Nowfoods, USA), composed of ten strains of bacteria (Lactobacillus acidophilus, Bifidobacterium lactis, Lactobacillus plantaLactobacillus paracasei, Bifidobacterium breve, Streotococcus thermophiles, Lactobacillus salivarius, and Bifidobacterium longum),

Locations

Country Name City State
Egypt Sara Maher Cairo

Sponsors (1)

Lead Sponsor Collaborator
Theodor Bilharz Research Institute

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

Sobocki BK, Kazmierczak-Siedlecka K, Folwarski M, Hawrylkowicz V, Makarewicz W, Stachowska E. Pancreatic Cancer and Gut Microbiome-Related Aspects: A Comprehensive Review and Dietary Recommendations. Nutrients. 2021 Dec 10;13(12):4425. doi: 10.3390/nu13124425. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Immunohistochemistry testing for immune cells infiltration and interferon-gamma expression Change in the percentage of infiltrating CD8T cells in the tumor tissue as well as the interferon-gamma in synbiotics group IHC testing for formalin fixed paraffin embedded block for all subjects 10 months from the beginning of the study, as we collected the all samples
Primary Inflammatory cytokines level A change in the inflammatory cytokines levels (IL 10, IL6, and IL 1 ß) in synbiotics-treated group with a significant difference rather the placebo and probiotics only treated groups 10 months after collection of all blood samples from included subjects
Primary Post-operative -non-infectious complications- improvement Testing the percentage of subjects having Anastomotic Leakage, Diarrhea, Abdominal distension 1-4 weeks post operative
Primary Post-operative -infectious complications improvement Testing the percentage of subjects having Bacteremia, Wound infection, Pneumonia, Urinary tract infection 1-4 weeks post operative
Primary Post-operative improvement days Number of days for first stool, stay in the hospital and return to usual activity first day post operative till 20 days
Primary Statistical analysis of the results To assess the significance of changes in the percentage of CD8 cells in the tissue in all subjected groups as well as the expression of Interferon-gamma protein. Also, the concentration of circulating cytokines including IL B, IL6, and IL 10.
Data were analyzed using statistical software package (IBM-SPSS) version 23 software. Kolmogorov-Smirnov test showed that the raw data were normally distributed. One ANOVA was applied to study the effect of treatment on the studied parameters. Two-way ANOVA was applied to study the effect of time and treatment on the studied parameters. The least significant difference (LSD) test was used to illustrate the statistical differences among the experimental groups. Duncan's test was used to illustrate the homogeneity among the different intervals. Data is displayed as mean ± standard error of the mean.
11 months from the beginning of the study
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