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Effect of Metoclopramide on the duration of spontaneous active phase of labor in primigravid women at the Jos University Teaching Hospital; a randomized, double blind, placebo controlled trial

Not Applicable
Not yet recruiting
Conditions
Labour
Registration Number
PACTR202401879224913
Lead Sponsor
Jos University teaching Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
88
Inclusion Criteria

1.Primigravidae at term with singleton pregnancy
2.Primigravidae at term with spontaneous onset of labour and foetus in longitudinal lie and cephalic presentation
3.Primigravidae at term with cervical os dilatation of 4cm
4.Primigravidae meeting the above criteria who give consent to be included in the study

Exclusion Criteria

1.Women who have had a previous delivery
2.Women who have progressed beyond 4cm cervical os dilatation
3.Women with any contraindication to vaginal delivery
4.Women with abnormal presentations, multiple pregnancies, cephalo-pelvic disproportion, maternal obesity, short stature or medical disorder in pregnancy
5.Women with previous uterine scars
6.Women with previous adverse drug reaction to metoclopramide or with contraindication to metoclopramide
7.Women taking medications with drug interaction to metoclopramide
8.Women presenting preterm in labour

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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