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Effectiveness of Castor Oil in Preventing Formal Induction of Labour in a Tertiary Institution

Effectiveness of Castor Oil in Preventing Formal Induction of Labour Among Pregnant Women at a Tertiary Institution in Abakaliki: A Randomized Controlled Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06841939
Enrollment
100
Registered
2025-02-24
Start date
2021-03-05
Completion date
2022-01-04
Last updated
2025-02-24

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

Conditions

Castor Oil, Prolonged Pregnancy

Keywords

Castor oil, Induction of labour, Prolonged pregnancy

Brief summary

This study demonstrated that castor oil was effective in reducing the need for formal induction of labour and the administration-delivery interval with minimal maternal side-effects, at an initial dose of 30ml and single repeat dose of 30ml.

Detailed description

Background: Pregnancy extending beyond 42 week is attended by maternal and perinatal complication including death. It is the commonest reason for induction of labour. Various agents have been used to induce labour but it is not without maternal and fetal side effects. Alternative agents such as castor oil have been widely used in clinical practice for induction of labour without any concrete evidence of effectiveness. Objective: To evaluate the effectiveness of castor oil in the prevention of formal induction of labour amongst pregnant mothers at Alex Ekwueme Federal University Teaching Hospital Abakaliki as well as to evaluate the possible maternal and fetal/ neonatal effects. Methods: This was a randomized controlled trial among pregnant women at Alex Ekwueme Federal University Teaching Hospital Abakaliki to verify the effectiveness of castor oil in the prevention of formal induction of labour at gestational ages between 41weeks and 0 days and 41 weeks and 2 days. One arm received 30ml of castor oil (Group A) and the other arm received 30ml of water (Group B). These doses were repeated once more after 24 hours if the patients failed to enter spontaneous labour. The data obtained was analyzed using IBM SPSS software (version 24, Chicago II, USA) and the intention to treat concept. A difference with a P value of ≤ 0.05 was taken to be of statistical significance.

Interventions

Participants recruited into this group had vaginal examinations conducted and it was confirmed that they were not in labour, Bishop's score was then documented. They were counselled to take 30 ml of castor oil under direct observation by the researcher and the time and date of administration documented. The participants' phone numbers and addresses were also recorded. Participants who fail to achieve labour within 24 hours had a repeat dose of 30 ml of castor oil.

OTHERWater

Participants recruited into this group had vaginal examinations conducted and it was confirmed that they were not in labour, Bishop's score was then documented. They were counselled to take 30 ml of water under direct observation by the researcher and the time and date of administration documented. The participants' phone numbers and addresses were also recorded. Participants who fail to achieve labour within 24 hours had a repeat dose of 30 ml of water.

Sponsors

Assumpta Nnenna Nweke
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

open label clinical superiority randomized controlled trial

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 44 Years
Healthy volunteers
Yes

Inclusion criteria

1. Gestational age of 41weeks+0day to 41weeks+2days 2. Pregnancies with cephalic presenting fetuses 3. Pregnant women with singleton fetus 4. Absence of contraindications to vaginal delivery 5. Absence of uterine contraction 6. Bishop score ≤ 5 7. Ultrasound confirmed GA in early pregnancy

Exclusion criteria

1. Pregnant women in latent phase of labour 2. Preterm or term premature rupture of membrane 3. Antepartum haemorrhage 4. Previous Caesarean section and myomectomy 5. Multiple gestation 6. Medical disorders of pregnancy 7. Unsure date

Design outcomes

Primary

MeasureTime frameDescription
formal Induction of labour24 hoursproportion of women who had formal induction of labour

Countries

Nigeria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026