Postpartum Period
Conditions
Interventions
This is a non-randomized, open clinical study. Women up to 19 years of age, who gave birth at the Women's Hospital, University of Campinas between July 2019 and April 2020, were invited to participate
Sponsors
Universidade Estadual de Campinas
Universidade Estadual de Campinas
Organon Brasil
Eligibility
Sex/Gender
Female
Age
10 Years to 19 Years
Inclusion criteria
Inclusion criteria: Adolescent postpartum until 19 years
Exclusion criteria
Exclusion criteria: Adolescent postpartum who do not wish to use any contraceptive method; who present absolute contraindication to the use of the contraceptive method chosen according to WHO or who are not able to attend childbirth review appointments.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: Around 90% of puerperal women will be satisfied with the subdermal implant, verified by calculating the risk of acceptance of the method, calculated by the prevalence rate with a 95% confidence interval, based on the finding of a variation of at least 5% in the pre- and post-intervention measurements. ;Outcome found 1: 91.4% of puerperal women were satisfied with the implant, as verified by calculating the risk of acceptance of the method, calculated by the prevalence rate with a 95% confidence interval, between the pre- and post-intervention periods. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected. | — |
Countries
Brazil
Contacts
Public ContactMariane;Mariane Barbieri;Barbieri
Universidade Estadual de Campinas;Universidade Estadual de Campinas
Outcome results
None listed