NCT06847373 Efficacy and Safety of Vitamin D Supplementation in Pediatric Patients with Obesity
| NCT ID | NCT06847373 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Coordinación de Investigación en Salud, Mexico |
| Condition | Vitamin D |
| Study Type | INTERVENTIONAL |
| Enrollment | 40 participants |
| Start Date | 2025-03-01 |
| Primary Completion | 2025-09-30 |
Eligibility & Interventions
Eligibility Fast-Check
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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 40 participants in total. It began in 2025-03-01 with a primary completion date of 2025-09-30.
⚠ 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
Introduction: Vitamin D deficiency is commonly observed in patients with obesity, primarily due to sequestration by adipose tissue. Recent research highlights the importance of this deficiency, showing a correlation between low vitamin D levels and mechanisms contributing to insulin resistance. Objectives: This study aims to compare the effects of supplementing with 4,000 IU of vitamin D versus 1,000 IU over six months on insulin resistance and the leptin/adiponectin ratio in school-aged children and adolescents with obesity. Materials and Methods: A controlled clinical trial will be conducted involving 40 children with obesity aged 10 to 18 years (BMI \>95th percentile). Participating children and their parents will undergo measurements such as weight, height, BMI, body fat, and Tanner stage. All participants will receive dietary and physical activity recommendations based on WHO guidelines. After initial assessments, participants will be randomly assigned to receive either 4,000 IU or 1,000 IU of vitamin D. They will be monitored monthly for capsule intake and adverse effects, with follow-up measurements of anthropometry, leptin, adiponectin, insulin \& lipid profile. Statistical Analysis: Baseline characteristics will be compared using t-Student or U-Mann Whitney tests, depending on variable distribution. The intervention's impact will be assessed by calculating deltas for body fat and biochemical measurements, with significance tested using paired t-tests or Wilcoxon tests. Covariance analysis (ANCOVA) will be used to adjust for confounding variables.
Eligibility Criteria
Inclusion Criteria: * Male and female participants. * Participants aged between 10 and 18 years. * Obesity as defined by a Body Mass Index (BMI) in the \>95th percentile according to the World Health Organization's age and sex-specific tables. * Willingness to participate in the study. * Residency in Mexico City. Exclusion Criteria: * Patients with comorbidities not attributable to obesity, such as chronic kidney disease, heart failure, liver cirrhosis, etc. * Patients with Prader-Willi syndrome, Albright's hereditary osteodystrophy, Borjesson-Forssman-Lehmann syndrome. * Patients currently taking vitamin supplements. * Patients undergoing pharmacological treatment for obesity. * Patients who already present insulin resistance and, although they have not previously received medication, are currently indicated for pharmacological treatment with metformin.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06847373 clinical trial?
This trial is open to participants of all sexes, aged 10 Years or older, up to 18 Years, studying Vitamin D. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06847373 currently recruiting?
Yes, NCT06847373 is actively recruiting participants. Contact the research team at zuritajn@gmail.com for enrollment information.
Where is the NCT06847373 trial being conducted?
This trial is being conducted at México, Mexico.
Who is sponsoring the NCT06847373 clinical trial?
NCT06847373 is sponsored by Coordinación de Investigación en Salud, Mexico. The trial plans to enroll 40 participants.