NL-OMON48381
Recruiting
Not Applicable
PRegnancy Outcomes and Maternal Insulin Sensitivity - PROMIS
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- niversitair Medisch Centrum Groningen
- Enrollment
- 130
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- Healthy singleton pregnant women (10\-12 weeks of gestation)
- •\- BMI \*25 kg/m2
- •\- Fasting Blood Glucose (FBG \*7\.0 mmol/l)
- •\- Dutch or English speaking
- •\- Written informed consent
Exclusion Criteria
- •\- Serious health complications (Hypertension, Hyperlipidemia, Asthma, Haemochromatosis) or medication use that influence the glucose metabolism or fetal growth (e.g. corticosteroids).
- •\- Multiple pregnancy
- •\- pre\-existing Diabetes type 1 and 2 defined as FBG \*7\.0 mmol/l or use of diabetes medication
- •\- Participation in any other studies involving the investigation of medication or nutritional products or antibiotic use in the two weeks prior to entry into the study
- •\- HIV/Hepatitis
- •\- Expectation of non\-compliance to the study protocol, among others, a fear of needles
- •\- Known allergies or intolerances for nutritional ingredients in the MTT
- •\- Psychological dysfunctions
Outcomes
Primary Outcomes
Not specified
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