PACTR202308835750161CompletedUnknown
Efficacy of paracetamol in the relief of pain in advanced labour in low resource settings: a randomized double-blind placebo-controlled study.
Olufunke Oso0 sites140 target enrollmentStarted: July 16, 2023Last updated:
Trial Snapshot
- Phase
- Unknown
- Status
- Completed
- Sponsor
- Enrollment
- 140
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 19 Year(s) to 44 Year(s) (—)
- Sex
- Female
Inclusion Criteria
- •Parturients,
- •Aged 18–35 years,
- •Spontaneous onset of labour at term (37–41 weeks + 6 days gestation),
- •Cervical dilatation of 6-7 cm
- •A single live fetus in cephalic presentation
- •Consent to participate in the study
Exclusion Criteria
- •Multiple pregnancy
- •Previous uterine scar
- •Cervical dilation = 5 and = 8cm at admission
- •Chronic or pregnancy-induced medical conditions
- •Presence of any contraindication to vaginal delivery
- •Fetal distress
- •Congenital malformations
- •Intrauterine growth restriction
- •Intrauterine fetal death
- •Allergy to paracetamol
- •Breech Presentation
- •Use of any other kind of analgesia before recruitment to the study
- •Non-consenting patient
Investigators
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