NCT05750342Completed
Clinical Trial to Analyze the Efficacy of a Supplement Extracted From Persimmon on Overweight / Obesity.
Randomized Clinical Trial to Analyze the Efficacy of a Supplement Extracted From Persimmon on Overweight / Obesity Grade I in Subjects With Body Mass Index Greater Than 25.
Source: ClinicalTrials.gov · Last updated 17 May 2024
Brief summary (registry, in English)
Randomized, controlled, double-blind clinical trial, with two parallel branches depending on the product consumed (experimental product and placebo product) and single-center, to measure the efficacy of a supplement extracted from Persimmon on overweight and obesity grade I in subjects with BMI over 25.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 80 (actual)
- First submitted
- 30 Jan 2023
- Start date
- 1 Feb 2023
- Primary completion date
- 28 Mar 2024
- Lead sponsor
- Universidad Católica San Antonio de Murcia
- Diseases
- Obesity
- NCT number
- NCT05750342
What you commit to
- Study type: Interventional
- Participants enrolled: 80
- From 1 Feb 2023 to the primary completion date, 28 Mar 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Subjects who have undergone major surgery in the last 3 months.
Other illness
- Subjects with acute diseases.
- Volunteers with a history or presence of chronic pulmonary disorders, hepatic, renal, hematological, gastrointestinal, endocrine, immunological, dermatological, urological, neurological, psychiatric, cardiovascular, or malignant tumor pathology or disease.
- Subjects with allergies or eating disorders.
Other
- Subjects undergoing treatment that may affect body weight.
- Subjects who quit smoking in the last 6 months or who intend to quit during the study.
- Volunteers who are participating in another study that involves blood draws or dietary intervention.
- Pregnant or breastfeeding women.
Who the study is looking for
- Subjects of both sexes aged 18-65 years.
- Subjects with a body mass index greater than 25 and less than 35.
- Volunteers able to understand the clinical study and willing to comply with the study procedures and the procedures and requirements of the study.
Age in the registry: 18 years to 65 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Catholic University of Murcia Coordinator of this site? Confirm its status | Murcia | Spain | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.