Clinical Trials Directory

Trials / Completed

CompletedNCT03541005

Evaluation of Obex® in Overweight and Obesity

Efficacy and Safety of the Obex® Nutritional Supplement in Overweight and Obese Subjects: Phase III.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
160 (actual)
Sponsor
Catalysis SL · Industry
Sex
All
Age
20 Years – 65 Years
Healthy volunteers
Not accepted

Summary

* Obesity is an important and growing worldwide * Obesity is highly related to the development of metabolic syndrome, diabetes, cardiovascular diseases and cancer * Diverse adverse events have been reported with the use of antiobesity drugs. * Several articles describe the beneficial effect of several specific components of the Obex® supplement on weight loss, in the reduction of waist circumference, suppression of appetite, decrease fasting glucose levels, improvement of insulin sensitivity and β cells function. * Therefore, the administration of Obex in overweight and obese patients could be an excellent strategy to induce weight loss and ameliorate the metabolic disturbances related to obesity and overweight.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTObexAfter concluded the six months of treatment, patients will be follow-up during six months without consumption of Obex
DIETARY_SUPPLEMENTPlaceboAfter concluded the six months of treatment, patients will be follow-up during six months without consumption of the placebo.

Timeline

Start date
2018-10-01
Primary completion
2019-09-01
Completion
2021-07-03
First posted
2018-05-30
Last updated
2021-10-21

Locations

1 site across 1 country: Cuba

Source: ClinicalTrials.gov record NCT03541005. Inclusion in this directory is not an endorsement.