A Study of the Effect of Probiotics on Gastrointestinal Function During Pregnancy
Status: | Recruiting |
---|---|
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 1/18/2019 |
Start Date: | January 9, 2018 |
End Date: | December 2020 |
Contact: | Courtney Overstreet |
Email: | hs-obgynresearch@ucdavis.edu |
Phone: | 916-734-6846 |
The purpose as well as the aim of this project is to understand the effect of probiotics on
gastrointestinal (GI) dysfunction such as nausea, vomiting, and constipation that are found
during the first and second trimesters of pregnancy.
The primary objective of this project is to uncover whether probiotics have an effect on GI
functional disorders.
The secondary objective is to identify the microbiota associated with probiotic intake.
The tested hypothesis is that gut microbiota influences the GI functions and may influence
constipation, nausea, and vomiting during pregnancy.
gastrointestinal (GI) dysfunction such as nausea, vomiting, and constipation that are found
during the first and second trimesters of pregnancy.
The primary objective of this project is to uncover whether probiotics have an effect on GI
functional disorders.
The secondary objective is to identify the microbiota associated with probiotic intake.
The tested hypothesis is that gut microbiota influences the GI functions and may influence
constipation, nausea, and vomiting during pregnancy.
Inclusion Criteria:
- First and second trimester healthy or low risk pregnant women who report
gastrointestinal disorders such as nausea, vomiting, and constipation
Definition of healthy or low risk pregnant women:
- Systolic blood pressure < 140 mmHg and diastolic blood pressure < 90 mmHg
- Hemoglobin ≥ 10.0 g/dL
- Have immunity against rubella (German measles)
- HIV negative
- Urine test shows no sign of kidney or urinary tract infection
- 27 weeks 6 days gestation or less with confirmed fetal heart beat
- Pregnant women age 18 and older
Exclusion Criteria:
- High risk pregnant women who have existing health conditions such as high blood
pressure, Type 1 diabetes, HIV positive, or are infected with Hepatitis B, Syphilis,
or other sexually transmitted diseases
- Pregnant women who have multiple gestations or a history of recurrent miscarriages
(more than two consecutive miscarriages)
- Had prior bariatric surgery
- Conceived through IVF program
- Pregnant women who have had severe weight loss (more than 5 pounds) during pregnancy.
[Note: Mild weight loss (2-3 pounds) due to nausea, vomiting, or loss of appetite is
considered normal.]
- Medical history of irritable bowel syndrome or other non-pregnancy related GI
dysfunction/disorder
We found this trial at
1
site
1 Shields Ave
Sacramento, California 95616
Sacramento, California 95616
(530) 752-1011
Principal Investigator: Albert Liu, MD
Phone: 916-734-6846
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