Clinical trial

Iron Metabolism in Obesity

Opening soon · Not applicable · 1 countries · Registry ID NCT07157332

Opening soonNot applicableObservational

What this study is about

This study consists of two phases and aims to understand how obesity and systemic iron deficiency affect iron accumulation in important organs such as the liver and heart, as well as oxidative stress in fat tissue cells. In Phase 1, researchers will compare individuals with obesity who have iron deficiency to those without, to see if there are differences in the amount of iron stored in the liver and heart, measured by magnetic resonance imaging (MRI), and in oxidative stress and labile iron in visceral and subcutaneous fat tissue, assessed through biopsies. Phase 2 is a six-month prospective cohort study following the same individuals after they undergo bariatric surgery, a weight-loss surgery. The goal is to evaluate whether weight and fat loss normalize iron accumulation in the liver and heart, reduce oxidative stress, improve systemic iron metabolism, enhance blood sugar control, support liver function, modulate chronic inflammation, and restore gut microbiota diversity. Researchers will compare these health changes between individuals with and without iron deficiency. The study includes adults aged 18 to 50 with obesity living in the metropolitan area of Monterrey, Mexico, who are scheduled for laparoscopic sleeve gastrectomy surgery and agree to participate. The findings could improve understanding of how iron metabolism interacts with obesity-related complications and may lead to better treatments and management strategies for people with obesity and iron deficiency.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to 50 Years
SexAll
Healthy volunteersNot accepted
ConditionObesity (Disorder)

Full registry criteria

Inclusion Criteria: * Male and female participants aged 18 to 50 years. * Premenopausal women (defined as no absence of menstruation in the past 12 months). * Body Mass Index (BMI) between 35 and 45 kg/m² at recruitment. * Scheduled to undergo bariatric surgery via sleeve gastrectomy or laparoscopic adjustable gastric banding (LAGB), with indications aligned with international guidelines. Bariatric surgery eligibility includes: 1. BMI between 35 and 45 kg/m² with the presence of obesity-related comorbidities (medical, physical, or psychosocial conditions), and a history of unsuccessful attempts at sustained weight loss through non-surgical means. 2. Adequately informed, understanding and accepting the potential risks and benefits of the procedure, and expressing commitment to adhere to long-term dietary and physical activity recommendations post-surgery. * Willing to maintain consistent dietary iron intake and refrain from taking any iron supplements other than those prescribed by the attending surgeon throughout the study duration. * Not pregnant during the study period or in the six months prior to enrollment, and not planning to become pregnant for at least 3 months after the final study visit (at 6 months). * Not breastfeeding in the six weeks prior to enrollment, nor planning to breastfeed during the study. * No significant weight loss (≥10% of body weight) in the six months prior to the pre-surgical evaluation. * Signed informed consent. * No night shift work during the two weeks prior to the baseline visit or at any point during the study (night shift defined as work performed between 12:00 AM and 6:00 AM). * Not engaging in strenuous physical activity ≥10 hours per week. Exclusion Criteria: * Participants who have undergone any bariatric procedure other than LAGB or sleeve gastrectomy. * Severe anemia (defined as hemoglobin \<100 g/L). * History of previous surgical obesity treatments. * Presence of significant medical conditions that may affect iron status or inflammatory markers independently of obesity, including but not limited to: cancer, HIV/AIDS, inflammatory bowel disease, gastrointestinal bleeding, rheumatoid arthritis, and chronic kidney disease (per investigator's judgment). * Diagnosed abnormalities in iron metabolism based on routine pre-surgical blood samples and unrelated to obesity (e.g., thalassemia). * History of frequent blood transfusions. * Chronic liver disease (e.g., alcoholic liver disease, hepatitis C-related liver disease). * Use of medications that could interfere with study measurements (per investigator's judgment). * Women consuming ≥14 alcoholic beverages per typical week or men consuming \>21 alcoholic beverages per typical week.

Treatments and study arms

Bariatric Sleeve Surgery

Procedure

Participants undergo a restrictive bariatric procedure called sleeve gastrectomy, performed by experienced surgeons. This procedure involves surgical reduction of the stomach size to aid in weight loss. The study observes outcomes related to iron metabolism, body composition, and biochemical markers over six months post-surgery. No additional interventions or treatments are applied as part of the study protocol; the surgery is part of routine clinical care.

Primary outcomes

Percentage of Body Weight Loss at 6 Months Post-SurgeryMeasured at baseline (pre-surgery) and 6 months post-surgery.

Proportion of initial body weight lost by each participant, calculated as ((initial weight - weight at 6 months) / initial weight) × 100. This measure is used to assess the effectiveness of bariatric sleeve surgery and to evaluate differences between participants with and without iron deficiency.

Study locations

1 locations were listed when this page was built. The first 40 are shown.

Fundación Santos y de la Garza Evia, IBP🇲🇽 San Pedro Garza García, Nuevo León, Mexico
Linda G Ortega Roldan, BScContact