Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with low risk primigravida between 37 to 41+6 weeks of gestation. Patients with singleton pregnancy with vertex presentation, occipito-anterior position, spontaneous labour, adequate pelvis presenting in active labour. Patients with intact amniotic membranes and cervical dilatation at 4cms. Patients willing to provide informed consent.
Exclusion criteria
Exclusion criteria: Patient for elective caesarean section. Patient who will be for induction of labour. Patient unwilling to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It measures the duration of labour (from the onset of active phase to delivery)Timepoint: The primary outcomes will be evaluated from active phase of labour until delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| Measure(s): Mode of delivery (spontaneous vaginal, instrumental vaginal, or cesarean section) Maternal outcomes: incidence of intrapartum complications (e.g., chorioamnionitis, postpartum hemorrhage) Neonatal outcomes: Apgar score at 1 & 5 minutes, need for NICU admission Maternal satisfaction with birthing experience (assessed postnatally before discharge)Timepoint: From onset of active phase until discharge of mother & newborn | — |
Countries
India
Contacts
N.K.P. Salve Institute of Medical Sciences and Research Centre