Skip to content

A Hospital-Based Randomized Controlled Trial — Comparing the Outcome of Delivery Between Upright (All Fours) and Supine Positions During Second Stage of Labour in Specialist Hospital, Owerri, Imo State, Nigeria.

Maternal and newborn outcome of upright (All Fours’) versus supine birthing positions in second stage in labouring women in Owerri using a randomized control trial

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
PACTR
Registry ID
PACTR202604495045431
Enrollment
245
Registered
2026-04-21
Start date
2026-03-23
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Comparing Birthing Positions during second stage of normal labour

Interventions

supine position

Sponsors

Claretian University of Nigeria Management
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: • Participants included primigravida and multigravida women between 37 and 41 weeks of gestation with low-risk pregnancies who met the following criteria: - Spontaneous onset of labour, induction, or augmentation - Fetus in cephalic presentation - Reassuring fetal heart rate - Adequate pelvis on clinical pelvimetry - Willingness to provide informed consent - Singleton pregnancy - No major medical or obstetric complications (e.g., preeclampsia, gestational diabetes, placenta previa) - No history of previous caesarean section - Maternal age 18–44 years

Exclusion criteria

Exclusion criteria: • Multiple pregnancy, non-cephalic presentation. • Known obstetric complications that mandate specific positioning or operative delivery (e.g., placenta praevia, cord prolapse). • Severe preeclampsia/eclampsia, active cardiac disease, or other maternal conditions where upright positioning is contraindicated. • Fetal distress at the time of randomization requiring immediate delivery. • Women who decline randomization • Women below 18 years and above 45years.

Design outcomes

Secondary

MeasureTime frame
• Mode of delivery: spontaneous vaginal, instrumental (forceps/vacuum), emergency cesarean. • Maternal: perineal trauma (graded 1–4), need for episiotomy, postpartum haemorrhage (blood loss estimate >500 ml), maternal pain score during second stage (validated scale, e.g., Visual Analogue Scale 0–10), maternal satisfaction (postnatal questionnaire within 24–48h). • Neonatal: Apgar score at 1 and 5 minutes; requirement for bag-mask ventilation or advanced resuscitation; NICU admission within 24 hours; birthweight; perinatal morbidity (birth trauma). • Adverse events: maternal falls, cord prolapse, shoulder dystocia, any unexpected serious adverse event (SAE) requiring transfer.

Primary

MeasureTime frame
The primary outcome is the time (in minutes) from full cervical dilatation (10 cm) to the delivery of the baby. This will be measured using a standard obstetric timer by the attending midwife or researcher. The duration will be compared between the upright (all-fours) position group and the supine position group to determine whether maternal positioning influences the length of the second stage of labour.

Countries

Nigeria

Contacts

Public ContactLekpa David

General enquiries

chinasaram2005@gmail.com2348035607640

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Jun 29, 2026