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OpenTrials
Completed

NCT Number: NCT01800760

Probiotics to Improve Women's Health

The purpose of the study is explore the effect of probiotics on plasma lipopolysaccharides (LPS) concentrations, as well as insulin and glucose levels, in obese women prior to and after dietary challenges (high carbohydrate meal, high fat meal).

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Arkansas Children's Nutrition Center

Little Rock, Arkansas, 72202, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • BMI=30-40 kg/m2
  • Healthy, age 18 or older
  • Not consuming yogurt or cultured milk regularly (</= 1x/wk) or any probiotic supplement

Exclusion criteria

  • Medical conditions or medications that may affect metabolism as determined by the PI.

Treatment and study plan

Probiotics

Dietary Supplement

Probiotics once a day for three weeks.

Primary outcomes

  1. Plasma LPS concentrations

    Time frame: five weeks

Secondary outcomes

  1. Glucose concentrations

    Time frame: five weeks

Sponsors and collaborators

Lead sponsor

Arkansas Children's Hospital Research Institute

Other

Registry information

Important dates

Study start
2012
Primary completion
2019
Study completion
2019
First posted
Feb 28, 2013
Registry last updated
Dec 20, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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