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Evaluation of effectiveness of Rectal Diaclofenac and Paracetamol suppositories in relieving labour pain among women in Calabar

Evaluation of effectiveness of Rectal Diaclofenac and Paracetamol suppositories in relieving labour pain among women in Calabar

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202407919661367
Enrollment
300
Registered
2024-07-24
Start date
2024-07-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Pregnancy and Childbirth Anaesthesia

Interventions

Labour Rectal Analgesia Study

Sponsors

Nil
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: All pregnant women from 37 weeks’ gestational age and above with singleton pregnancy and fetus in cephalic presentation that are admitted into the labour ward for vaginal delivery or induction of labour shall be included in the study.

Exclusion criteria

Exclusion criteria: The pregnant women with the following conditions would be excluded from the study. These include women with multiple gestation, abnormal foetal lie such as transverse or oblique lie, uterine masses such as fibroids, antepartum haemorrhage, fetal congenital anomaly, polyhydramnios, and oligohydramnios. Others are preterm labour, pre-labour rupture of membranes, and pregnant women who are unsure of their LMP or no dating ultrasound scan done before 13 weeks’ gestational age. Also, pregnant women that present in advanced first stage of labour or second stage of labour shall be excluded from the study.

Design outcomes

Primary

MeasureTime frame
The primary outcome will be to compare the differences in the mean pain scores across the groups and maternal satisfaction ratings after intervention. The baseline pain score before drug administration shall be assessed within 10 minutes before the drug is administered. After drug administration, the pain score shall be assessed in the following intervals, 30 minutes, 1 hour, 2 hours, 6 hours and 24 hours.

Secondary

MeasureTime frame
The secondary outcome will be to compare the differences in maternal and perinatal outcomes such as duration of labour, caesarean delivery, genital tear, febrile illness, time of initiation of breastfeeding and self care. Also symptoms like vomiting or urinary problem. The perinatal outcome include apgar scores, febrile illness, admission to neonatal intensive care unit.

Countries

Nigeria

Contacts

Public ContactGabriel Adim

Hospital Administrator

kebyayi@gmail.com+2347037291111

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026