Predicting Adverse Pregnancy Outcomes (PAPO) Study: An observational study to determine factors in both male and female partners to predict healthy pregnancies and adverse pregnancy outcomes

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ANZCTR

Registry ID

ACTRN12609000254291

Acronym

PAPO

Enrollment

750

Registered

2009-05-13

Start date

2008-10-01

Completion date

Unknown

Last updated

2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Investigating possible causes or predictors of adverse pregnacy outcomes.

Interventions

Dietary, lifestlye, genetic and circulating (blood) factors will be observed once before pregnancy (if posible) and again at 12 weeks gesation in the mother. Fathers will have blood taken only at one time point. Pregnancy Outome data will be collected within 6 weeks of particpants giving birth.

Eligibility

Sex/Gender

All

Age

18 Years to 55 Years

Healthy volunteers

Yes

Inclusion criteria

Recruit before 12 weeks gestation, Consent to participate

Exclusion criteria

Serious medical illness, lack of informed consent

Outcome results