Safety and Efficacy Study of a Food Supplement for Pregnant and Lactating Women

Oriflame Cosmetics

Status

Withdrawn

Conditions

Anaemia

Treatments

Dietary Supplement: Food supplement

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT02190565

2014/815-31/4

Details and patient eligibility

About

The purpose of this study is to determine whether a food supplement consisting of vitamins, minerals and fish oil taken during and after pregnancy can decrease the need for additional iron supplementation due to anemia during pregnancy, and optimize levels of nutritional markers such as vitamin D and docosahexaenoic acid (DHA, an omega 3 fatty acid) in maternal blood and breast milk, compared to placebo.

Full description

200 healthy, pregnant women will be randomized to receive either active or placebo at their first visit to the pre-natal centres. They will be monitored at regular intervals, blood samples will be taken and they will be asked about compliance and any adverse reactions.

Approx 8 weeks after delivery, the women will come to the pre-natal centres for a check-up. During this visit, a blood sample will be drawn and a breast milk sample will be collected.

The blood samples will be analysed for haemoglobin, serum ferritin, vitamin D and DHA. The breast milk samples will be analysed for vitamin D and DHA.

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Healthy pregnant women aged 18-40 years with a body mass index (BMI) above 18.5 and below 35 kg/m2 who visit pre-natal clinics (midwife centres) to register.
Nulliparous and multiparous women.
The women must be able to understand verbal and written information in Swedish to give an informed consent to participate in the study.

Exclusion criteria

Women below the age of 18 or above 40 years old.
Women with a BMI below 18.5 or above 35 kg/m2.
Women with any form of anaemia as diagnosed at the first visit to the prenatal clinic.
Women expecting two or more babies.
Women who have undergone bariatric surgery.
Women on medication with pharmaceuticals that could affect the result of the study, e.g., vitamin K antagonists.
Women who are allergic to any of the components of WellnessPack mama, e.g., fish.
Women who suffer from drug or alcohol abuse.
Women who suffer from known severe eating disorders.
Women who suffer from chronic diseases that could affect gastrointestinal absorption and metabolism.
Women who want to continue or start using similar food supplements in addition to WellnessPack mama/placebo, unless recommended by a physician or midwife, will be excluded from the study.
Upon miscarriage or transfer to prenatal care specialist, the subject is excluded from the study.