Custom vitamins for bariatric patients: do they outperform standard multis?
NCT ID NCT07021170
First seen Jun 26, 2026 · Last updated Sep 03, 2026 · Updated 2 times
Summary
This study tests whether specialized bariatric supplements (Elan Believe, Compass, Supreme) prevent vitamin and mineral deficiencies after weight-loss surgery better than standard over-the-counter multivitamins. Over 600 adults undergoing sleeve gastrectomy, gastric bypass, or one-anastomosis bypass will be followed for 12 months. The goal is to see if tailored formulations improve nutrient levels and patient compliance.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- specialized bariatric multivitamin supplements (Elan Believe, Elan Compass, Elan Supreme)
- What this could lead to
- If successful, this could show that tailored supplements are more effective than standard multivitamins at preventing nutrient deficiencies after bariatric surgery.
- What could go wrong
- This is a Phase 4 trial, so the supplements are already on the market. The main risk is that the specialized formulas may not prove significantly better than standard options, or that side effects like gastrointestinal discomfort could affect adherence.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
624 people
The number who actually took part.
- Started
-
Jun 2025
- Finished
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Jun 2026
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 years
- Sex
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Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Eligible participants must be adults: * Aged 18 to 65 years * Capable of providing informed consent * Willing to comply with study procedures and follow-up visits over 12 months. * Candidates must have no prior history of MBS or gastrointestinal surgery and must be scheduled for one of the three aforementioned primary procedures. * Both male and female patients will be considered, and no restrictions will be placed based on ethnicity or socioeconomic status. Exclusion Criteria: Exclusion criteria include: * The presence of chronic conditions that may independently affect micronutrient metabolism or absorption, such as chronic kidney disease, inflammatory bowel disease, or hepatic insufficiency. * Additional exclusion criteria include pregnancy or lactation at the time of enrollment * Plans for pregnancy within the study period * Active malignancy * Any use of investigational drugs or supplements within the past 30 days. * Patients undergoing revisional bariatric surgery or conversion procedures will also be excluded.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
The surgical department of Medical Research Institute Hospital, Alexandria University
Alexandria, Alexandria Governorate, 21531, Egypt
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Other studies related to the condition(s) this trial covers.
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