Efficacy of a Novel Multivitamin-Mineral Supplement in Preventing Vitamin Deficiency in Postoperative Bariatric Patients
Primary Purpose
Bariatric Surgery Candidate
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
AquaVanta Chewable Tablet
Flinstones Complete
Nature Made Calcium Softgels
Nature Made Calcium Softgels
Twin Labs Iron Caps
Rexall Vitamin B12 Tablet
Sponsored by
About this trial
This is an interventional prevention trial for Bariatric Surgery Candidate
Eligibility Criteria
Inclusion Criteria:
- Ages 18 - 65 years of age
- Meet appropriate criteria for Roux-en-Y gastric bypass (RYGB) surgery as determined by the Principal Investigator at The John's Hopkins Center for Bariatric Surgery (JHCBS)
Exclusion Criteria:
- Allergy to a component of the formulations
- Recent (last 3 months) use of a dietary supplement other than a standard non-bariatric specific multivitamin supplement
- Documented levels of fat-soluble vitamins (A,D,E,K) or iron above the normal range
- Pregnant or lactating
- Expected poor compliance with medical regimen as assessed by JHCBS clinic care providers
Sites / Locations
- The John's Hopkins Center for Bariatric Surgery (JHCBS)
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Novel Multivitamin/Mineral Supplement
Standard of care supplement
Arm Description
These subjects will be given a novel multivitamin/mineral supplement post RYGB bariatric surgery for 6 months duration.
These subjects will be given the standard recommended regimen at Johns Hopkins Bayview Medical Center post RYGB bariatric surgery for 6 months duration.
Outcomes
Primary Outcome Measures
Plasma vitamin and mineral levels
Secondary Outcome Measures
Questionnaire regarding the palatability of the formulation and the ease of administration of the formats and dosing schedule
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01475617
Brief Title
Efficacy of a Novel Multivitamin-Mineral Supplement in Preventing Vitamin Deficiency in Postoperative Bariatric Patients
Official Title
Efficacy of a Novel Multivitamin-Mineral Supplement in Preventing Vitamin Deficiency in Postoperative Bariatric Patients
Study Type
Interventional
2. Study Status
Record Verification Date
January 2015
Overall Recruitment Status
Completed
Study Start Date
November 2011 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
June 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yasoo Health
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Approximately 33% of the US adult population can be classified as obese based on body mass index. This epidemic of obesity has resulted in over 200,000 bariatric surgeries performed every year for the treatment of "clinically severe obesity". Roux-en-Y gastric bypass (RYGB) is the most common bariatric procedure performed in the United States and has both restrictive and malabsorptive components. Despite the success of this procedure in creating long lasting weight loss, vitamin and iron deficiencies are common and can lead to significant morbidity if not appropriately addressed. Despite the American Association of Clinical Endocrinologists, The Obesity Society, and American Society for Metabolic & Bariatric Surgery Medical Guidelines that include vitamin and mineral supplementation recommendations, there has been very little prospective research conducted to assess the efficacy and compliance of these micronutrient interventions.
This prospective randomized controlled clinical study will evaluate the efficacy of a novel vitamin/mineral supplement in decreasing micronutrient deficiencies in post operative bariatric patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bariatric Surgery Candidate
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
61 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Novel Multivitamin/Mineral Supplement
Arm Type
Experimental
Arm Description
These subjects will be given a novel multivitamin/mineral supplement post RYGB bariatric surgery for 6 months duration.
Arm Title
Standard of care supplement
Arm Type
Active Comparator
Arm Description
These subjects will be given the standard recommended regimen at Johns Hopkins Bayview Medical Center post RYGB bariatric surgery for 6 months duration.
Intervention Type
Dietary Supplement
Intervention Name(s)
AquaVanta Chewable Tablet
Intervention Description
AquaVanta Chewable Tablet (proprietary formulation of vitamin and minerals) 2 times a day for 6 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Flinstones Complete
Intervention Description
Flinstones Complete Multivitamin 2 times a day for 6 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Nature Made Calcium Softgels
Intervention Description
Nature Made Calcium Softgels (Calcium Carbonate 600 mg and Vitamin D 200 mg) three times a day for 6 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Nature Made Calcium Softgels
Intervention Description
Nature Made Calcium Softgels (Calcium Carbonate 600 mg and Vitamin D 200 mg) three times a day for 6 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Twin Labs Iron Caps
Intervention Description
Twin Labs Iron Caps (Ferrous Fumarate) 18 mg per day for menstruating women for 6 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Rexall Vitamin B12 Tablet
Intervention Description
Rexall Vitamin B12 Tablet (Cyanocobalamin 500 mcg)per day for 6 months
Primary Outcome Measure Information:
Title
Plasma vitamin and mineral levels
Time Frame
3 and 6 months compared to baseline
Secondary Outcome Measure Information:
Title
Questionnaire regarding the palatability of the formulation and the ease of administration of the formats and dosing schedule
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Ages 18 - 65 years of age
Meet appropriate criteria for Roux-en-Y gastric bypass (RYGB) surgery as determined by the Principal Investigator at The John's Hopkins Center for Bariatric Surgery (JHCBS)
Exclusion Criteria:
Allergy to a component of the formulations
Recent (last 3 months) use of a dietary supplement other than a standard non-bariatric specific multivitamin supplement
Documented levels of fat-soluble vitamins (A,D,E,K) or iron above the normal range
Pregnant or lactating
Expected poor compliance with medical regimen as assessed by JHCBS clinic care providers
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kimberley Steele Steele, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The John's Hopkins Center for Bariatric Surgery (JHCBS)
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21224-2780
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
29500675
Citation
Perin J, Prokopowicz G, Furtado M, Papas K, Steele KE. A Randomized Trial of a Novel Chewable Multivitamin and Mineral Supplement Following Roux-en-Y Gastric Bypass. Obes Surg. 2018 Aug;28(8):2406-2420. doi: 10.1007/s11695-018-3177-0.
Results Reference
derived
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Efficacy of a Novel Multivitamin-Mineral Supplement in Preventing Vitamin Deficiency in Postoperative Bariatric Patients
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