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AzTrials

Lifestyle-related ConditionLEGUMINIBUSNCT05999136

Effects of Pulses Through the Gut Microbiome and Bioavailability of Bioactive Compounds

A study testing Pulses diet, Plant proteins diet and Habitual diet in people with Lifestyle-related Condition, run by Paola Vitaglione at 1 site in Italy.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this clinical trial is to investigate the effects of replacing red meat with pulses, on cardiometabolic health and gut microbiome in individuals with unhealthy habits and sedentary lifestyles at high risk for cardiovascular diseases. The main questions it aims to answer are: 1. Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Lifestyle-related Condition
What is being tested?
Pulses diet, Plant proteins diet and Habitual diet
Could I receive a placebo?
No, everyone receives an active treatment
How many people
84 participants
Where
1 siteItaly
Study dates
10 Jan 2024to 20 Dec 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • men and women aged 18-65;
  • 20 ≤ BMI ≤ 35 kg/m2;
  • habitual diet characterized by ≥ 3 medium servings of fresh red meat or processed meat (equivalent to a portion weight of 100g of fresh meat and 50g of cured meats);
  • habitual diet without probiotics, functional foods, and/or any type of food supplements;
  • low level of physical activity (sedentary lifestyle);
  • signing the informed consent form and expressing consent for the processing of personal data.

Who cannot join

  • Food allergies and intolerances, such as celiac disease, lactose intolerance, and others;
  • Gastrointestinal disorders of any kind;
  • Significant medical conditions;
  • Pregnancy or breastfeeding;
  • Hypertriglyceridemia (Triglycerides > 200 mg/dL);
  • Hypercholesterolemia (Cholesterol > 200 mg/dL);
Show all 13Show fewer
  • Diabetes (Blood glucose ≥ 126 mg/dL);
  • Hypertension (Blood pressure > 140/90 mm Hg);
  • Weight loss ≥ 3 kg in the past 2 months prior to the study;
  • Use of any medication at enrollment and in the 2 months prior to the study;
  • Regular diet rich in fruits and vegetables;
  • Consumption of alcohol equivalent to or exceeding 3 glasses of wine per day;
  • Concurrent participation in other clinical trials.

Trial locations and contacts

1 site in 1 country.

Italy1 site
  • Department of Agricultural Sciences, Federico II University

    Portici, 80055

Other trials in Italy

About this study

Official title: Discovering the Effects of Pulses Through the Gut Microbiome and Bioavailability of Bioactive Compounds

The goal of this clinical trial is to investigate the effects of replacing red meat with pulses, on cardiometabolic health and gut microbiome in individuals with unhealthy habits and sedentary lifestyles at high risk for cardiovascular diseases. The main questions it aims to answer are:

  1. How does the substitution of red meat with pulses affect some markers of cardiovascular risk?
  2. How does this dietary intervention influence the composition and function of the gut microbiome, nutritional status, well-being indices, and biomarkers related to metabolic, oxidative, inflammatory, immune, and intestinal permeability status?
Read more

Participants will:

  • be assigned to either the Pulses Diet (PulD) group or the Plant Proteins Diet (PPD) group or the Habitual diet (HabD) group;
  • follow their habitual diet (HabD) or the prescribed dietary plan designed on individual habitual diet to be isocaloric and isoprotein but replacing red meat with pulses (PulD group) or a combination of pulses and plant-based meat substitutes (PPD group);
  • keep their physical activity levels unchanged during the entire intervention period;
  • be required to complete 7-day food diaries and associated questionnaires on appetite, along with additional questionnaires related to physical activity levels, overall well-being, mood, sleep quality, stool frequency and consistency at each nutritional intervention time-point.

Researchers will compare PulD, PPD, and HabD to assess if the dietary interventions have an impact on cardiometabolic health and gut microbiome.

Read the detailed description

Legumes are recognized for their distinctive nutritional profile, rich in plant-based proteins, low-glycemic-index carbohydrates, fiber, B vitamins, minerals, and polyphenols. Due to their protein content and amino acid composition, legumes in combination with grains can effectively replace meat and its derivatives. Despite worldwide nutritional guidelines recommending legumes as the predominant source of dietary protein, the consumption of red meat and meat products remains high and may have negative consequences for public health. Indeed, epidemiological evidence indicates that long-term consumption of increasing amounts of red and processed meats is associated with a higher risk of mortality, cardiovascular diseases, colon cancer, and type 2 diabetes. Furthermore, a recent study has shown that higher intake of red meat and choline is associated with higher concentrations of trimethylamine-N-oxide (TMAO), a gut microbiota byproduct that has been associated with a higher incidence of adverse cardiovascular events. Numerous research studies indicate that the consumption of plant-based foods brings health benefits for humans and supports the recommendation of international guidelines to modify dietary habits towards a diet richer in plant-based products. In addition, epidemiological studies show a possible association between high legume consumption and a decrease in coronary heart disease and colorectal adenoma, while the evidence for a protective role of legumes against cardiovascular diseases is less strong due to heterogeneity in results and/or potential confounding factors. The ability of legumes to reduce cardiometabolic risk factors is also supported by various scientific evidence from clinical trials. These studies demonstrate that legume consumption has a positive effect on lipid profile, glucose metabolism, blood pressure, body weight, oxidative stress, and inflammatory status.

Despite the recognized health benefits of consuming legumes regularly, there is still a limited understanding of the underlying physiological mechanisms that drive these positive effects. An observational study conducted in Italy shed some light on this issue by demonstrating that individuals who closely adhere to the Mediterranean diet, which emphasizes reducing red meat consumption and increasing the intake of fruits, vegetables, and legumes, have gut microbiota characterized by a higher abundance of fiber-degrading bacteria. These individuals also exhibit higher levels of short-chain fatty acids in their feces and lower concentrations of TMAO in their urine. Furthermore, a randomized controlled trial conducted on individuals at risk of cardiovascular diseases due to an unhealthy lifestyle revealed that shifting from a typical Western diet to a more Mediterranean-like pattern led to an increase in the presence of fiber-degrading bacterial species in the gut microbiota. This dietary change also resulted in elevated circulating microbial metabolites associated with improved inflammatory status. While there is still a lack of comprehensive in vivo studies assessing the bioavailability of nutrients from legumes, a few clinical trials have investigated the influence of legumes on the intestinal microbiome. Nevertheless, the available literature indicates that legumes have the ability to influence the human microbiota. However, it is important to note that the specific effects of legumes on the microbiota can vary significantly across different studies, making it difficult to generalize these findings to all types of legumes.

In this framework, the present project will focus on the evaluation of the effect of replacing red meat with pulses (PulD) or a combination of pulses and plant-based meat substitutes (PPD) on the cardiometabolic health of individuals with unhealthy habits and sedentary lifestyles via the modification of intestinal microbial communities. Additionally, it seeks to investigate the effects on health outcomes, with a primary focus on evaluating changes in inflammatory, oxidative, immune, and hormonal status. The study will include the establishment of a 2-month dietary intervention with an isocaloric and isoprotein pulses diet (PulD) and a plant proteins diet (PPD). Coupled with detailed host phenotyping and gut microbiota profiling during and after the intervention, this will allow assessment of the causal effects of a diet rich in plant-based proteins (mainly from pulses) and the gut microbiome in populations at high risk for cardiovascular disease (CVD).

The potential eligibility of subjects to participate in this study will be assessed through pre-recruitment questionnaires. These questionnaires will collect personal and socio-demographic data of volunteers, general health information (including anthropometry, health status, medical history, smoking and alcohol consumption habits), details about individual dietary habits using the Food Frequency Questionnaire (FFQ), information about eating behavior through the Three Factor Eating Questionnaire (TFEQ), and levels of physical activity using the International Physical Activity Questionnaire (IPAQ). Subjects in the PulD group and PPD group will be assigned a personalized diet prepared on the basis of own eating habits as established by 7-day food diary recalls. Energy values and whole macronutrient composition of habitual diets will be kept unchanged during PulD and PPD intervention. However, changes in carbohydrate (dietary fibre vs. starch), dietary fat (saturated vs. mono/polyunsaturated fatty acids), and protein (vegetable vs. animal) composition will be applied as a consequence of replacing meat with pulses (PulD group) or with a mix of pulses and plant-based meat substitutes (PPD group). Control subjects will not change their habitual diet (HabD) during intervention. All subjects will be requested not to change physical activity levels during the 8 weeks intervention period. Compliance will be assessed every 2 weeks with a phone interview in order to evaluate the dietary intake and physical activity during the previous week. At each intervention time-point (baseline, 4 weeks, 8 weeks), for the nutritional check, subjects will complete 7-day food diaries and associated questionnaires on appetite (Visual Analog Scale, VAS) related to the previous week before the nutritional analysis. Additionally, measurements of blood pressure, weight, circumferences (waist and hips), and body composition through bioimpedance testing will be conducted. During the intervention period, subjects will be asked to fill out the International Physical Activity Questionnaire (IPAQ), questionnaires on quality of life (QoL), on depression, anxiety and stress (DASS), the King's Stool Chart (KSC) to evaluate frequency, weight, and consistency of feces, along with the Pittsburgh Sleep Quality Index (PSQI) to evaluate the quality of sleep.

Further analysis of compliance will be conducted based on metabolomics, allowing discrimination of animal/vegetable protein intake. Metabolomes (well known to reflect both diet and microbial metabolism) will also be compared between categories in order to identify protective or risk profiles using both bioinformatics and chemometrics approaches. Metagenomes will be analyzed following Standard Operating Procedures (SOPs) utilized in landmark studies already published. Comparison of predefined groups of individuals will allow identification of microbial genes that have different abundance in the groups. Furthermore, genes will be associated with continuous variables of clinical and nutritional interest (e.g., intake of specific dietary components, insulin sensitivity) by covariance analysis. Concatenated datasets of physiological output data, metagenomic and metabolome profiles from the intervention studies will be used to predict subsets of features by multivariate analysis (PLS-DA) that can classify subjects according to their relative adherence to a PulD or PPD. The profile will be used to probe the microbiome for specific alterations as a function of the interventions.

The sample size needed to detect an effect of PulD and/or PPD on individual TMAO levels is defined based on previous study from Crimarco and colleagues. It was calculated that a sample of 28 participants per group would allow detecting a minimum difference of approximately -1.3 μM (-38%) in TMAO and approximately -0.9 mM (-18%) in cholesterol between each of the 2 test treatments vs. control and between the two test treatments, with a power of 80% and an α-error 0.017 to account for multiple comparisons (T-test).

Being tested
Pulses diet, Plant proteins diet, Habitual diet
Keywords
Gut microbiome, Legumes, Pulses, Plant proteins, Cardiovascular diseases, Red meat substitution, Protein transition, Overweight, Obesity
Medical subject headings
Mental Disorders, Cardiovascular Diseases, Overweight, Obesity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Pulses dietOther

    Subjects in the PulD group will be assigned a personalized diet prepared based on their own eating habits as established by 7-day food diary recalls. Energy values of habitual diets will be kept unchanged during the PulD intervention. The diet will be characterized by isocaloric and isoprotein substitutions, replacing habitual servings of red meat or processed meat with servings of pulses.

  • Plant proteins dietOther

    Subjects in the PPD group will be assigned a personalized diet prepared based on their own eating habits as established by 7-day food diary recalls. Energy values of habitual diets will be kept unchanged during the PPD intervention. The diet will be characterized by isocaloric and isoprotein substitutions, replacing habitual servings of red meat or processed meat with a mixture of pulses and plant-based meat substitutes.

  • Habitual dietOther

    Control subjects will not change their habitual diet during intervention. All subjects will be requested not to change physical activity levels during the 8 week intervention period.

Study groups in NCT05999136
Study groupRoleWhat they receive
Pulses Diet (PulD)ExperimentalSubjects will follow a Pulses-enriched diet for 2 months.
Receives: Other: Pulses diet
Plant Proteins Diet (PPD)ExperimentalSubjects will follow a Plant protein-enriched diet for 2 months.
Receives: Other: Plant proteins diet
Habitual Diet (HabD)Active comparatorSubjects will follow a habitual diet for two months.
Receives: Other: Habitual diet

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Changes in fasting total cholesterol concentration

    Measure of serum total cholesterol concentration (mg/dL serum)

    Measured: 2 months

  2. Changes in plasma TMAO concentration

    Measure of plasma TMAO concentration (μmol/L plasma)

    Measured: 2 months

Secondary outcomes (43)
  1. Changes in faecal microbiome

    Measure of faecal microbiome

    Measured: 2 months

  2. Changes in urinary TMAO concentration

    Measure of urinary TMAO concentration (mmol/mol creatinine)

    Measured: 2 months

  3. Changes in urinary polyphenols concentration

    Measure of urinary polyphenols concentration (ng/mg creatinine)

    Measured: 2 months

  4. Changes in urinary urolithin concentration

    Measure of urinary urolithin concentration (ng/mg creatinine)

    Measured: 2 months

  5. Changes in urinary betaine concentration

    Measure of urinary betaine concentration (mmol/mol creatinine)

    Measured: 2 months

  6. Changes in urinary carnitine concentration

    Measure of urinary carnitine concentration (mmol/mol creatinine)

    Measured: 2 months

  7. Changes in urinary choline concentration

    Measure of urinary choline concentration (mmol/mol creatinine)

    Measured: 2 months

  8. Changes in urinary tryptophan betaine concentration

    Measure of urinary tryptophan betaine concentration (mmol/mol creatinine)

    Measured: 2 months

  9. Changes in urinary indican concentration

    Measure of urinary indican concentration (mg/g creatinine)

    Measured: 2 months

  10. Changes in urinary creatinine concentration

    Measure of urinary concentration (mg/dL)

    Measured: 2 months

  11. Variation of complete blood count

    Measure of Red blood cell (RBC) count (number of cells/mm3); Hemoglobin (Hb) concentration (g/dL); Hematocrit (HCT) percentage (%); White blood cell (WBC) count (number of cells/mm3); Platelet (PLT) count (number of cells/mm3).

    Measured: 2 months

  12. Variation of blood iron status biomarkers

    Measure of blood concentrations (mg/dL) of iron, ferritin, total transferrin

    Measured: 2 months

  13. Variation of vitamin B status

    Measure of blood folic acid and vitamin B12 concentrations (ng/mL)

    Measured: 2 months

  14. Variation of individual hormonal status

    Measure of plasma glucagon-like peptide 1 (GLP-1), Glucose-dependent Insulinotropic Peptide (GIP), Glucagon, Leptin, Ghrelin, C-peptide concentrations (pg/mL plasma)

    Measured: 2 months

  15. Variation of plasma endocannabinoids concentration

    Measure of plasma endocannabinoids concentration (ng/mL)

    Measured: 2 months

  16. Variation of plasma N-acylethanolamines concentration

    Measure of plasma N-acylethanolamines concentration (ng/mL)

    Measured: 2 months

  17. Changes in plasma betaine concentration

    Measure of plasma betaine concentration (μmol/L plasma)

    Measured: 2 months

  18. Changes in plasma carnitine concentration

    Measure of plasma carnitine concentration (μmol/L plasma)

    Measured: 2 months

  19. Changes in plasma choline concentration

    Measure of plasma choline concentration (μmol/L plasma)

    Measured: 2 months

  20. Changes in plasma bioactive peptides concentration

    Measure of plasma bioactive peptides concentration (ng/mL plasma)

    Measured: 2 months

  21. Changes in plasma bile acids concentration

    Measure of plasma bile acids concentration (ng/mL plasma)

    Measured: 2 months

  22. Variation of plasma oxidative stress biomarkers

    Measure in plasma of: TBARS concentration (µM); nitrotyrosine (N-Tyr) concentration (OD/mL); 8-hydroxy-2-deoxyguanosine (8-OHdG) concentration (ng/mL)

    Measured: 2 months

  23. Variation of plasma antioxidant enzyme activities

    Measure of plasma superoxide dismutase (SOD) activity (U/mL); catalase activity (nmol/min/mL); glutathione peroxidase (GPx) activity (nmol/min/mL)

    Measured: 2 months

  24. Variation of serum dipeptidyl peptidase-IV (DPP-IV) concentration and activity

    Measure of serum dipeptidyl peptidase-IV (DPP-IV) concentration (ng/mL) and activity (IU/L)

    Measured: 2 months

  25. Variation of serum Triglycerides concentration

    Measure of serum triglycerides concentration (mg/dL serum)

    Measured: 2 months

  26. Variation of serum LDL- and HDL-cholesterol concentrations

    Measure of serum LDL-, HDL-cholesterol concentrations (mg/dL serum)

    Measured: 2 months

  27. Variation of serum glucose concentration

    Measure of serum glucose concentration (mg/dL)

    Measured: 2 months

  28. Variation of serum insulin concentration

    Measure of serum insulin concentration (μU/mL serum)

    Measured: 2 months

  29. Variation of serum Insulin-like Growth Factor-1 (IGF-1) concentration

    Measure of serum IGF-1 concentration (ng/mL)

    Measured: 2 months

  30. Variation of serum C-reactive protein (CRP) concentration

    Measure of serum CRP concentration (mg/L)

    Measured: 2 months

  31. Variation of serum zonulin concentration

    Measure of serum zonulin concentration (ng/mL)

    Measured: 2 months

  32. Changes in immune state blood markers

    Measure of monocyte polarization (Arbitrary Units) of Cluster of Differentiation (CD) 86, Tumor Necrosis Factor alpha (TNFα), inducible Nitric Oxide Synthase (iNOS), CD36, CD11c, CD169, CD206, CD163, CD68, CD11b, CD16, e CD14

    Measured: 2 months

  33. Variation of erythrocytes antioxidant enzymes activity

    Measure in erythrocytes of: superoxide dismutase (SOD) activity (U/mL); catalase activity (nmol/min/mL); glutathione peroxidase (GPx) activity (nmol/min/mL); glutathione reductase (GR) activity (U/mL)

    Measured: 2 months

  34. Changes in body weight

    Measure of body weight (kg) in fasting subjects

    Measured: 2 months

  35. Changes in body mass index

    Calculation of body mass index (kg/m2) by using the formula weight in kilograms divided by height in meters squared.

    Measured: 2 months

  36. Changes in waist and hip circumferences

    Measure of waist circumference (cm) at the midpoint between the lower margin of the least palpable rib and the top of the iliac crest.

    Measure of hip circumference (cm) around the widest portion of the buttocks.

    Measured: 2 months

  37. Changes in blood pressure

    Measure of systolic pressure and diastolic pressure in millimetres of mercury (mmHg) by using a digital sphygmomanometer

    Measured: 2 months

  38. Changes in body composition

    Body composition (kg body fat mass, body fat-free mass and total body water) is determined by conventional bioelectrical impedance analysis with a single-frequency 50 kilohertz (kHz) bioelectrical impedance analyzer in the postabsorptive state (fasting subjects) and after being in the supine position for 20 min. Body composition data will be calculated from bioelectrical measurements and anthropometric data by using validated predictive equations.

    Measured: 2 months

  39. Variation of hunger, fullness and satiety sensation scores

    Measures of hunger, fullness and satiety sensations over the day reported by subjects by using hunger Visual Analogue Scales (VAS) 0-10 centimeters. Changes in these scores may reflect potential effects of dietary intervention in modulating hunger, fullness and satiety.

    Measured: 2 months

  40. Changes in stool weight, consistency and frequency

    Measure of stool weight, frequency and consistency by mean of King's Stool Chart (KSC) filled out by subjects. The chart comprises three categories of stool weight : <100 g, 100-200 g, >200 g. The chart comprises four categories of stool consistency: hard and formed, soft and formed, loose and unformed, liquid. Fecal frequency is incorporated by recording the code of each feces passed over a 24 hour period.

    Measured: 2 months

  41. Assessment of diet composition

    Measure of individual's usual food consumption through Food Frequency Questionnaires (FFQ) by querying the frequency (times/week) and amount (g) at which the respondent consumed food items based on a predefined food list.

    Measured: 2 months

  42. Changes in physical activity level

    Measurement of an individual's physical activity level (MET min/week) through the International Physical Activity Questionnaire (IPAQ), which assesses the frequency (times/week) and duration (min) of different activities such as walking, moderate-intensity exercises, vigorous-intensity exercises, and sitting time.

    Measured: 2 months

  43. Variation of wellbeing status

    Estimate of wellbeing status by mean of quality of life (QoL) questionnaire, which is based on Short Form-12 Health Survey (SF-12), a self-report form of subjective health. Physical and Mental Health Composite Scores (PCS \& MCS, arbitrary units) are computed using the scores of twelve questions and range from 0 to 100, where a zero score indicates the lowest level of health measured by the scales and 100 indicates the highest level of health.

    Measured: 2 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Aug 2023
  2. Study start10 Jan 2024
  3. Primary completion20 Dec 2024
  4. Study completion20 Dec 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
84 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05999136
Sponsor's protocol ID
DE LEGUMINIBUS
Acronym
LEGUMINIBUS
Status last verified
Jun 2026
First submitted
13 Aug 2023
Last updated
22 Jun 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: All individual participant data that underlie the results reported in the publication will be shared after deidentification

Publications

  • Crimarco A, Springfield S, Petlura C, Streaty T, Cunanan K, Lee J, Fielding-Singh P, Carter MM, Topf MA, Wastyk HC, Sonnenburg ED, Sonnenburg JL, Gardner CD. A randomized crossover trial on the effect of plant-based compared with animal-based meat on trimethylamine-N-oxide and cardiovascular disease risk factors in generally healthy adults: Study With Appetizing Plantfood-Meat Eating Alternative Trial (SWAP-MEAT). Am J Clin Nutr. 2020 Nov 11;112(5):1188-1199. doi: 10.1093/ajcn/nqaa203.

    PubMed 32780794
  • Meslier V, Laiola M, Roager HM, De Filippis F, Roume H, Quinquis B, Giacco R, Mennella I, Ferracane R, Pons N, Pasolli E, Rivellese A, Dragsted LO, Vitaglione P, Ehrlich SD, Ercolini D. Mediterranean diet intervention in overweight and obese subjects lowers plasma cholesterol and causes changes in the gut microbiome and metabolome independently of energy intake. Gut. 2020 Jul;69(7):1258-1268. doi: 10.1136/gutjnl-2019-320438. Epub 2020 Feb 19.

    PubMed 32075887

Questions about this trial

What is this clinical trial studying?

A study testing Pulses diet, Plant proteins diet and Habitual diet in people with Lifestyle-related Condition, run by Paola Vitaglione at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Changes in fasting total cholesterol concentration (time frame: 2 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05999136, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jun 2026.

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