nil
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion Criteria 1.Willingness and consent to participate in the study 2.Nulliparity 3.Term gestation (37-42weeks) 4.Singleton viable intrauterine pregnancy 5.Parturients presenting before 4cm cervical dilatation 6.Cephalic presentation 7.Intact membranes 8.HIV negative Parturient
Exclusion criteria
Exclusion criteria: Exclusion Criteria 1.Any contraindication to vaginal delivery 2.Ruptured membrane 3.Multiparas 4.Multiple pregnancy 5.HIV positive parturient 6.Advanced labour or parturients who present after 4cm cervical dilatation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the primary outcome measure was the duration of first stage of labour in both arms of the study | — |
Secondary
| Measure | Time frame |
|---|---|
| the secondary outcome measures includes rate of cervical dilatation, duration of second and third stage labour, route of delivery, rate of birth asphyxia, rate of caesarean section and the need for neonatal admission. | — |
Countries
Nigeria
Contacts
principal investigator and specialist gynaecologist at Federal Medical centre Asaba