- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02912416
Efficacy of Probiotics on Iron Status During Pregnancy
March 3, 2020 updated by: Probi AB
Determine the effect of probiotics on improving iron status in a population of healthy, pregnant women.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
326
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Malmö, Sweden, 205 12
- CuraÖresund
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 42 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Healthy, pregnant women, aged 18-42 years, with a singleton gestation
- Inclusion at 10-12 weeks of gestation
- BMI ≥ 18 and ≤ 30 at baseline
- Provide signed and dated informed consent form
- Willing to comply with all study procedures
Exclusion Criteria:
- Serum ferritin level <20 µg/L or Hb<110 g/L at baseline (visit 1)
- Chronic diseases associated with anemia
- Known Thalassemia
- Hyperemesis gravidarum
- Chronic gastrointestinal disease (inflammable bowel diseases; Crohn's disease, Ulcerative Colitis; diarrheal disease)
- Known gluten intolerance, lactose intolerance, milk protein allergy
- Taking antibiotics within four weeks before inclusion
- Blood or plasma donation within three (3) months prior to baseline
- History of any clinically significant disease or disorder which, in the opinion of the Investigator, may either put the subject at risk because of participation in the study, or influence the results or the subject's ability to participate in the study
- Smoking or use of nicotine-containing products (currently or during the last three [3] months)
- History of alcohol abuse, or excessive intake of alcohol, as judged by the Investigator
- Hypersensitivity to any of the ingredients in the study products
- Any other reason for exclusion, as judged by the Investigator
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Probiotics
Capsule with probiotics
|
|
Placebo Comparator: Placebo
Capsule with placebo
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Serum ferritin level
Time Frame: Week 28 of gestation
|
Week 28 of gestation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 9, 2016
Primary Completion (Actual)
November 11, 2018
Study Completion (Actual)
November 11, 2018
Study Registration Dates
First Submitted
September 21, 2016
First Submitted That Met QC Criteria
September 21, 2016
First Posted (Estimate)
September 23, 2016
Study Record Updates
Last Update Posted (Actual)
March 4, 2020
Last Update Submitted That Met QC Criteria
March 3, 2020
Last Verified
March 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ProIron 16
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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