Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07427914

Effectiveness and Safety of Benemix® in Constipation

Evaluation of the Effectiveness and Safety of Benemix®, a Functional Food, in the Management of Constipation in Adults

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Universidad de Antioquia · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to find out whether the functional food Benemix® helps treat constipation in adults and whether it is safe to use. The main questions this study aims to answer are: Does Benemix® help improve bowel movement frequency and consistency in adults with constipation? What medical problems, if any, do participants experience while taking Benemix®? Adults with constipation will take Benemix® every day for 15 days. During the second week, participants will have either an in-person clinic visit or a telemedicine appointment for checkups and tests. Participants will also receive follow-up phone calls to record: * daily treatment adherence * signs and symptoms * the number of bowel movements each day.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTBenemix®, a functional food composed of turmeric, onion, magnesium, and lactose-free, skimmed milk powderBenemix® is a functional food formulation designed to support intestinal health and relieve functional constipation in adults. It contains a combination of turmeric (Curcuma longa), onion (Allium cepa), magnesium, and lactose-free skimmed milk powder. Participants will consume one oral serving of Benemix® once daily for 15 consecutive days. The product is provided as a powdered formulation that must be reconstituted in water or milk prior to consumption. Benemix® differs from other dietary interventions by combining bioactive compounds from turmeric and onion, which have anti-inflammatory and digestive properties, with magnesium, known for its osmotic laxative effect. The lactose-free dairy base is intended to improve tolerability in individuals who are sensitive to lactose. All participants will receive instructions on proper preparation and use of the product. Treatment adherence will be monitored through follow-up phone calls and daily symptom diaries.

Timeline

Start date
2026-07-01
Primary completion
2026-08-01
Completion
2026-12-01
First posted
2026-02-23
Last updated
2026-02-23

Source: ClinicalTrials.gov record NCT07427914. Inclusion in this directory is not an endorsement.