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Use of Probiotics to Aid in Weight Loss (Probiotics)

Primary Purpose

Weight Loss

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Probiotics
Placebo
Sponsored by
Prisma Health-Upstate
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Weight Loss focused on measuring Weight loss, Probiotics, Gastric Bypass

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Male or Female at least 18 years of age
  • Signed informed consent
  • Willingness to take a supplement once a day for 12 weeks
  • Undergoing a RNYGB (gastric bypass) procedure
  • Willingness to complete quality of life questionnaire and hair loss survey

Exclusion Criteria:

  • Pregnant Female
  • Lactating Female
  • Male or Female less than 18 years of age
  • Patients on chronic antibiotic treatment (prescribed more than 2 courses of antibiotics over the 12 week study period)
  • Patients who have demonstrated medical therapy non-compliance past or present

Sites / Locations

  • Greenville Hopsital System - Division of Bariatric and Minimal Access Surgery

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Probiotics

Placebo

Arm Description

Patients treated with a probiotic (in capsule form) once daily for 12 weeks

Patients treated with a placebo (in capsule form) identical to that of the probiotic capsule once daily for 12 weeks

Outcomes

Primary Outcome Measures

Percentage of weight loss in post operative gastric bypass patients.
Percentage of weight loss will be measured using the The RJL Systems' Quantum IX on all patients for bioelectrical impedance analysis (BIA) to assess human body composition before beginning supplementation and at the end of the 12 week period. The Tanita system will be used as the back-up machine throughout the study as applicable.

Secondary Outcome Measures

Impact of study medication (Probiotics vs. Placebo) on overall Gastrointestinal Health
Use of the validated quality of life survey: GIQOLI (Gastrointestinal Quality of Life Index)

Full Information

First Posted
September 29, 2011
Last Updated
April 8, 2014
Sponsor
Prisma Health-Upstate
Collaborators
Xymogen, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01445704
Brief Title
Use of Probiotics to Aid in Weight Loss
Acronym
Probiotics
Official Title
Use of Probiotics to Aid in Weight Loss
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
June 2010 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
January 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Prisma Health-Upstate
Collaborators
Xymogen, Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the success of daily supplementation of multiple probiotic bacterial cultures over 12 weeks in increasing the percentage of excess weight loss in the RNYGB (Gastric Bypass) weight loss population.
Detailed Description
Hypothesis: The daily supplementation of a probiotic will increase weight loss compared to a placebo supplement in the post-operative gastric bypass patients. Study Design: All patients in this study will be scheduled to undergo the RNYGB (Gastric Bypass) procedure to assist in weight loss. Patients in this study will be randomized to one of two groups: Group 1 (Probiotics) or Group 2 (Placebo). Patients will begin supplementation at the beginning of their 4 week pre-surgery Optifast© 800 diet. All patients will take supplements for a total of 12 weeks. Nutritional education and support will be provided to each patient enrolled in the study. Weight loss will be measured using a machine that measures body composition. All patients will complete a quality of life questionnaire with regard to gastrointestinal health and a hair loss survey pre treatment and at the end of the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Weight Loss
Keywords
Weight loss, Probiotics, Gastric Bypass

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
151 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Probiotics
Arm Type
Experimental
Arm Description
Patients treated with a probiotic (in capsule form) once daily for 12 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Patients treated with a placebo (in capsule form) identical to that of the probiotic capsule once daily for 12 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotics
Intervention Description
The probiotic supplementation will use lactic acid bacteria in the "ProbioMax DF™" supplement from Xymogen, Inc. This preparation consists of a four-strain probiotic with 100 billion CFU per vegetable capsule. The strains included are Lactobacillus acidophilus La-14, Bifidobacterium lactis HN019, Lactobacillus planarum Lp-115, and Bifidobacterium longum B1-05.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
The placebo supplementation is identical-looking to the capsule of the probiotic supplementation.
Primary Outcome Measure Information:
Title
Percentage of weight loss in post operative gastric bypass patients.
Description
Percentage of weight loss will be measured using the The RJL Systems' Quantum IX on all patients for bioelectrical impedance analysis (BIA) to assess human body composition before beginning supplementation and at the end of the 12 week period. The Tanita system will be used as the back-up machine throughout the study as applicable.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Impact of study medication (Probiotics vs. Placebo) on overall Gastrointestinal Health
Description
Use of the validated quality of life survey: GIQOLI (Gastrointestinal Quality of Life Index)
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Male or Female at least 18 years of age Signed informed consent Willingness to take a supplement once a day for 12 weeks Undergoing a RNYGB (gastric bypass) procedure Willingness to complete quality of life questionnaire and hair loss survey Exclusion Criteria: Pregnant Female Lactating Female Male or Female less than 18 years of age Patients on chronic antibiotic treatment (prescribed more than 2 courses of antibiotics over the 12 week study period) Patients who have demonstrated medical therapy non-compliance past or present
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John D Scott, M.D.
Organizational Affiliation
Prisma Health-Upstate
Official's Role
Principal Investigator
Facility Information:
Facility Name
Greenville Hopsital System - Division of Bariatric and Minimal Access Surgery
City
Greenville
State/Province
South Carolina
ZIP/Postal Code
29607
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
10067658
Citation
Anderson JW, Gilliland SE. Effect of fermented milk (yogurt) containing Lactobacillus acidophilus L1 on serum cholesterol in hypercholesterolemic humans. J Am Coll Nutr. 1999 Feb;18(1):43-50. doi: 10.1080/07315724.1999.10718826.
Results Reference
background
PubMed Identifier
11393194
Citation
Vanderhoof JA. Probiotics: future directions. Am J Clin Nutr. 2001 Jun;73(6):1152S-1155S. doi: 10.1093/ajcn/73.6.1152S.
Results Reference
background
PubMed Identifier
11271697
Citation
Kopp-Hoolihan L. Prophylactic and therapeutic uses of probiotics: a review. J Am Diet Assoc. 2001 Feb;101(2):229-38; quiz 239-41. doi: 10.1016/S0002-8223(01)00060-8.
Results Reference
background
Citation
Woodard G.; Peraza J.; Downey J.; Encarnacion B.; Morton J. 343 Probiotics Improve Weight Loss, GI-Related Quality of Life and H2 Breath Tests After Gastric Bypass Surgery: A Prospective Randomized Trial. Gastroenterology. 2008 April; Vol. 134 (4), suppl. 1, pp. A-846.
Results Reference
background
PubMed Identifier
7749697
Citation
Eypasch E, Williams JI, Wood-Dauphinee S, Ure BM, Schmulling C, Neugebauer E, Troidl H. Gastrointestinal Quality of Life Index: development, validation and application of a new instrument. Br J Surg. 1995 Feb;82(2):216-22. doi: 10.1002/bjs.1800820229.
Results Reference
background
Links:
URL
http://www.cdc.gov/obesity/data/index.html
Description
Center for Disease Control and Prevention

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Use of Probiotics to Aid in Weight Loss

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