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Clinical Trials/PACTR202407919661367
PACTR202407919661367RecruitingUnknown

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

il0 sites300 target enrollmentStarted: July 14, 2024Last updated:

Trial Snapshot

Phase
Unknown
Status
Recruiting
Sponsor
Enrollment
300

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

  • 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

  • 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.

Investigators

Sponsor
il

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