Parturition
Conditions
Interventions
Control group: 15 pregnant women induced with 25mg of misoprostol will be seen according to the usual care provided by the pre-delivery service at the Maternity Hospital of the University Hospital Lau
Sponsors
Universidade Federal de Pernambuco
Universidade Federal de Pernambuco
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Pregnant women who are 18 years of age or older; Labor induced by the drug Misoprostol (25mcg, vaginally); Single pregnancy; Pregnant woman generating a live fetus; The pregnant women who will compose the study group must present cervical dilation greater than or equal to 5 cm at the beginning of the intervention
Exclusion criteria
Exclusion criteria: Maternal physical and / or mental disability; Fetal malformation; Women in an expulsive period of labor.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Identify the increase in the number of vaginal births verified by recording in the medical record | — |
Secondary
| Measure | Time frame |
|---|---|
| Decrease the number of doses of the drug used during induction ;Decrease the total time of induction of labor in the study group evaluated from the time between the beginning and the end of the induction;Decrease the duration of the active phase and the expulsive period of labor in the study group;Decrease the level of pain assessed using the Visual Analogue Scale;Minimize the occurrence of grade 3 or 4 laceration identified in the medical record;Provide 5 minute high APGAR of the newborn | — |
Countries
Brazil
Contacts
Public ContactMilene Almeida
Outcome results
None listed