Management of Delivery Clinical Trial
— PLADRAINAGEOfficial title:
Effectiveness of Placental Drainage in the Third Stage of Labor: a Randomized Clinical Trial
The purpose of this study is to determine if placental drainage shortens third period of labor and reduces postpartum blood lost.
| Status | Completed |
| Enrollment | 226 |
| Est. completion date | May 2013 |
| Est. primary completion date | May 2013 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Female |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Low risk pregnant women - Pregnancy at term - Women at low risk for assisted labor / delivery and postpartum care. - Live Fetus Exclusion Criteria: - Women under 18, mentally handicapped and indigenous; - Women who agreed to participate signed the Informed Consent, but evolved to cesarean section or instrumental delivery by forceps; - Instrumental Delivery by forceps or c-section |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Brazil | IMIP | Recife | Pernambuco |
| Lead Sponsor | Collaborator |
|---|---|
| Instituto Materno Infantil Prof. Fernando Figueira |
Brazil,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Duration of the third period of labor | Time from delivery of the baby to the delivery of the placenta | Six hours | No |
| Secondary | Postpartum blood loss | Volume of blood lost 24 hours after birth | 24 hours | No |
| Secondary | PPH | Postpartum hemorrhage | 24 hours | No |
| Secondary | Need of uterotonics | use of aditional uterotonics ( prophylkatic use not included) | 24 hours | No |
| Secondary | Need of blood transfusions | Need of blood transfusions | until discharge | No |