None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Apparent healthy pregnant women, 18-40 years old, recruited early in 1st trimester pregnancy
Exclusion criteria
Exclusion criteria: Subjects > 13 weeks of gestation at recruitment, Subject with twin or multiple pregnancies, Pregnant women with chronic morbidity or on long term medications or positivity for hepatitis B (HBsAg), HIV or syphilis (VDRL) infections, Subjects anticipating moving out of study site for delivery, Pregnant women not willing to participate in the infusion protocol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measurement and comparison of methionine and arginine kinetics in the 1st and 3rd trimester of pregnancy among the 2 groups of pregnant womenTimepoint: during pregnancy | — |
Secondary
| Measure | Time frame |
|---|---|
| gestational weight gain birth weightTimepoint: during pregnancy at birth | — |
Countries
India
Contacts
St Johns Research Institute