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Recruiting NCT06193577

NCT06193577 Effect of Phaseolus Vulgaris L. Dry Extract on the Modulation of Weight and Metabolic Parameters

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Clinical Trial Summary
NCT ID NCT06193577
Status Recruiting
Phase
Sponsor IBSA Farmaceutici Italia Srl
Condition Weight Loss
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2023-11-08
Primary Completion 2025-06-30

Eligibility & Interventions

Sex Male only
Min Age 18 Years
Max Age 60 Years
Study Type INTERVENTIONAL
Interventions
Phaseolus Vulgaris L. Dry ExtractPlacebo

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 60 participants in total. It began in 2023-11-08 with a primary completion date of 2025-06-30.

⚠ 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

Evaluation of the efficacy of Phaseolus vulgaris L. dry extract on weight modulation.

Eligibility Criteria

Inclusion Criteria: * Male subjects aged between 18 and 60 years * BMI between 25 and 35 kg/m2 * Habitual consumption of three main meals a day * Stable body weight during the 3 months prior to enrollment * Commitment to adhere to the diet and avoid the use of other weight loss products during the study * Commitment not to change lifestyle significantly for the entire duration of the study. * Signing of informed consent Exclusion Criteria: * Hypergonadotropic hypogonadism and hypogonadotropic hypogonadism * Diabetes mellitus * Smoking \> 10 cigarettes/day * Alcohol \> 2 alcohol units/day (equal to 24 g of ethanol) * History of eating disorders during the 12 months prior to enrollment * Use of any drug or product to treat obesity (e.g. meal replacements) * Presence of acute or chronic gastrointestinal diseases * Active use of drugs that could influence the functions: gastrointestinal (e.g. laxatives, etc.), insulin (insulin sensitizers, etc.) and/or testicular (hormones, substances that influece testosterone production * Known sensitivity to the ingredients of the preparation * Any other clinical condition judged by the investigator to be incompatible with participation in the trial

Contact & Investigator

Central Contact

Carmelo Gusmano, MD

✉ carmelo.gusmano@yahoo.it

📞 +393891136444

Principal Investigator

Aldo Calogero, Prof.

PRINCIPAL INVESTIGATOR

Università di Catania

Frequently Asked Questions

Who can join the NCT06193577 clinical trial?

This trial is open to male participants only, aged 18 Years or older, up to 60 Years, studying Weight Loss. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06193577 currently recruiting?

Yes, NCT06193577 is actively recruiting participants. Contact the research team at carmelo.gusmano@yahoo.it for enrollment information.

Where is the NCT06193577 trial being conducted?

This trial is being conducted at Catania, Italy.

Who is sponsoring the NCT06193577 clinical trial?

NCT06193577 is sponsored by IBSA Farmaceutici Italia Srl. The principal investigator is Aldo Calogero, Prof. at Università di Catania. The trial plans to enroll 60 participants.

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