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Fentanyl versus pethidine for labour analgesia among parturients at the University of Abuja Teaching Hospital: A randomized controlled trial.

Comparing the effectiveness and safety of fentanyl with pethidine for pain relief during Labour

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
PACTR
Registry ID
PACTR202505569677581
Enrollment
120
Registered
2025-05-08
Start date
2025-05-01
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Pregnancy and Childbirth Labour pain

Interventions

B. Pethidine group

Sponsors

Tsiterimam Thomas Sambo
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Parous Parturient 2. Pregnant women at 37 weeks of gestation to 42 weeks who are admitted at cervical dilatation of 4-7cm. 3. Single viable fetus with cephalic presentation.

Exclusion criteria

Exclusion criteria: 1. Women with contraindication to vaginal delivery (history of Antepartum haemorrhage in the index pregnancy, Fetal macrosomia, Pelvic deformity, and non-reassuring fetal heart) 2. Pregnant women with a previously scarred uterus (post-myomectomy, post-Cesarean) 3. History of allergy to the study drugs or any opiates. 4. History of medical disorders (hypertension, Diabetes, Sickle cell disease, etc.)

Design outcomes

Primary

MeasureTime frame
1. The mean pain score. 2. Maternal satisfaction with pain relief

Secondary

MeasureTime frame
1. Maternal side effects: fainting, nausea and vomiting, respiratory depression (respiratory rate < 12), hypotension (blood pressure < 90/60 mmHg), and bradycardia (heart rate < 60 beats/min). 2. Neonatal outcome (Apgar scores at one and five minutes, need for resuscitation, and admission to neonatal intensive care unit) 3. Need for extra analgesia 4. Duration of labour

Countries

Nigeria

Contacts

Public ContactAnthony Dennis Isah

Supervisor

denisanthonyisah@yahoo.com+2348061109664

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Feb 4, 2026