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Vitamin and Mineral Supplementation Post Bariatric Surgery

Not Applicable
Conditions
Complications of Other Bariatric Procedure
Interventions
Dietary Supplement: Vitamins and Minerals
Registration Number
NCT02817256
Lead Sponsor
United Arab Emirates University
Brief Summary

Bariatric surgery is emerging as an essential treatment option for the management of obesity and its associated comorbidities. Many patients present for surgery have pre-existing low blood vitamin levels, thus all bariatric surgical procedures compromise nutrition to varying extents, and may present potential threat of micronutrient deficiencies. Therefore, long term nutritional monitoring and follow-ups are vital components of all bariatric surgical patients. However, there are no current standard practices in United Arab Emirates (UAE) for the biochemical monitoring and replacement of essential micronutrients in patients undergoing bariatric surgery particularly the most performed Sleeve Gastrectomy. Medical practice guidelines recommend nutritional care however, the dose and route of administration supplementation after surgery based on randomized controlled trials is not yet established. Till tow no scientific study has been performed on monitoring vitamins and minerals levels following bariatric surgery among UAE population. Therefore, present study is aimed to determine the dose and route of administration of vitamins and minerals in improving the micronutrient deficiencies post-operatively. Two standard different dosage forms (oral /parenteral) of vitamins and minerals will be given to the patients who had undergone sleeve gastrectomy at Tawam Hospital. The dosages of the supplementations are within the international recommendations and patients will be followed up closely for a period of one year. The effect of nutritional deficiencies on micronutrient level and quality of life (QOL) will be assessed. This will help the medical practitioners to prove the optimal possible nutrition for patients.

Detailed Description

The study will be conducted in Tawam Hospital where patients come for their routine bariatric surgery. A written informed consent will be taken from all the patients willing to participate in the study. Patients would be informed about the objectives / goals of the study.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
105
Inclusion Criteria
  • Age: 18-60 years;
  • No medical or psychiatric contraindications;
  • BMI>35 kg/m2 with co-morbidities or BMI > 40 kg/m2 prior to the bariatric surgery.
Exclusion Criteria
  • • Documented severe micronutrient deficiency that require treatment

    • Documented poor compliance;
    • History of in concordance to medication;
    • Inflammatory bowel disease, malignant or debilitating medical conditions;
    • Known hemoglobinopathies or those diagnosed with pernicious anaemia;
    • Known history of kidney renal stones or history of hypercalcaemia;
    • Significant longstanding medical complications that affect micronutrient status;
    • Severe psychiatric illness;
    • Women who are lactating, pregnant or planning pregnancy.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Group A, 'vitamins and minerals'Vitamins and Minerals"Ergocalciferol , Vitamin B12, Calcium /D ", "Iron" or "Centrium". Ergocalciferol 300,000 IM - Every 3 months Oral Vitamin B12 tablets daily (500mcg) Calcium /D Tab 600-200mg Centrium -1 Tablet Daily Mineral: Iron preparation - Daily (47mg)
Group B, 'vitamins and minerals'Vitamins and Minerals"Ergocalciferol , Vitamin B12, Calcium /D ", "Iron" or "Centrium". Centrium - 1 Tablet daily Ergocalciferol 50000 IU once every two weeks Vitamin B12 1000mcg IM every three months Calcium /D Tab 600-200mg Minerals: Iron preparation - Daily (47mg)
Primary Outcome Measures
NameTimeMethod
monitor the levels of micronutrients of Iron1 year

Change in micronutrients level of Iron

Secondary Outcome Measures
NameTimeMethod
complications resulting from IM injections1 year

Number of complications resulting from IM injections

monitor the levels of Vitamin A1 year

Change in level of Vitamin A

monitor the levels of Vitamin D1 year

Change in level of Vitamin D

monitor the levels of Serum folate1 year

Change in level of Serum folate

monitor the levels of Serum methyl malonate1 year

Change in level of Serum methyl malonate

monitor the levels of uric acid1year

Change in level of uric acid

monitor the levels of calcium1 year

Change in level of calcium

monitor the levels of Vitamin B121 year

Change in level of Vitamin B12

Trial Locations

Locations (2)

Faculty of Medicine and Health Sciences

🇦🇪

Al Ain, United Arab Emirates

Faculty of Medicine and Health Sciences UAE University

🇦🇪

Al Ain, AB, United Arab Emirates

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