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Recruiting NCT07069751

NCT07069751 A Prospective Multicenter Study of the Effects of Plant-based Diets on Gut Microbiome and Derived Metabolites in Patients Affected by Smoldering Multiple Myeloma

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Clinical Trial Summary
NCT ID NCT07069751
Status Recruiting
Phase
Sponsor Ciceri Fabio
Condition Smoldering Multiple Myeloma (SMM)
Study Type INTERVENTIONAL
Enrollment 62 participants
Start Date 2025-10-31
Primary Completion 2027-06

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 75 Years
Study Type INTERVENTIONAL
Interventions
diet rich in fiber

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 62 participants in total. It began in 2025-10-31 with a primary completion date of 2027-06.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Our overarching hypothesis is that plant-based diets will induce beneficial modifications of the gut microbiota favoring short fatty acid (SCFA)-producing commensals and a more advantageous CD8/Th17 ratio in sMM patients, thus preventing evolution to MM. Goal of this national, prospective, multicenter study is to demonstrate that plant-based diets substantially modify the gut microbiome inducing increased production of SCFAs in patients affected by sMM. The study will involve up to 62 patients affected by sMM. 56 Enrolled and eligible patients will be encouraged to consume a balanced diet rich in fiber for the entire duration of the trial (i.e., 12 weeks). Patients will choose among a list of different diet plans or individual food according to the personal tastes and preference. Free outpatient medical visit will be performed at enrollment and at week 12, and nutritional counseling will be given at the time of enrollment, one month later and on demand. As in line with routine diagnosis and follow-up of for patients affected by sMM, the investigators will collect bone marrow aspirates and peripheral blood at the time of screening, for plasma, serum, and peripheral blood mononuclear cells (PBMCs), while stool samples will be collected immediately before diet initiation. The investigators will also collect stool samples 4 and 12 weeks after diet initiation, and peripheral blood at 12 weeks after study initiation (as per routine clinical follow-up of this patient population). Dietary measurements will be conducted along the entire duration of the nutritional regimen by questionnaires. Biological paired comparison will be conducted between data obtained from samples collected at time 0 and samples collected 4 and 12 weeks later.

Eligibility Criteria

Inclusion Criteria: 1. Participant is willing and able to give informed consent for participation in the study. 2. Confirmed diagnosis of sMM according to IMWG criteria 3. Absence of features of symptomatic or active myeloma requiring treatment (myeloma-defining events). 4. Aged ≥18 and \</= 75 years 5. Participant is willing to comply with all study-related procedures. 6. ECOG performance status of 0-1. Exclusion Criteria: 1. Non-Caucasian subjects. Racial disparities in all stages of the disease characterize MM, and Blacks have an increased MGUS and MM risk and higher mortality rate than Whites. 2. Patients that already follow a whole food plant-based diet (≥ 40g/die;ovo-lacto-vegetarian or processed junk food vegan diets are not excluded). These patients likely should already have high SCFA levels in their gut. 3. Legume allergy. 4. Severe allergies such as anaphylactic shock to nuts (specifically cashews). 5. Concurrent participation in weight loss/dietary/exercise programs because of potential conflicts between the concurrent diet and high-fiber diet. 6. Enrollment onto any other therapeutic investigational study. 7. Concurrent pregnancy. 8. Ongoing treatment for HBV, HCV or HIV. 9. If in the opinion of the investigator there maybe any concerns regarding the ability of the patient to complete the study safely or any contraindications. 10. Heavy drinker (defined as \>2 drinks per day or \>14 drinks per week). 11. Current self-reported illicit drug use (e.g., heroin, cocaine not marijuana). 12. Subjects that did not accept to sign the informed consent. 13. Subjects reporting infectious diseases requiring antibiotic therapy in the previous three months, ongoing antibiotic therapy, or prophylaxis. Antibiotic therapy dramatically modifies the composition of the gut microbiota. 14. Subjects affected by autoimmune diseases except for thyroiditis, and patients affected by small and large intestine dysfunctions (i.e., inflammatory bowel disease). 15. Gammopathy-associated conditions beyond sMM (e.g. amiloydosis, POEMS, LCDD, etc).

Contact & Investigator

Central Contact

Tommaso Perini

✉ ciceri.clinicaltrials@hsr.it

📞 02-26436615

Frequently Asked Questions

Who can join the NCT07069751 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Smoldering Multiple Myeloma (SMM). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07069751 currently recruiting?

Yes, NCT07069751 is actively recruiting participants. Contact the research team at ciceri.clinicaltrials@hsr.it for enrollment information.

Where is the NCT07069751 trial being conducted?

This trial is being conducted at Milan, Italy, Bari, Italy, Milan, Italy, Milan, Italy and 1 additional location.

Who is sponsoring the NCT07069751 clinical trial?

NCT07069751 is sponsored by Ciceri Fabio. The trial plans to enroll 62 participants.

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