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Metoclopramide Versus Hyoscine Butylbromide in Shortening Duration of First Stage of Labour

U

Uwakwe Emmanuel Chijioke

Status and phase

Unknown
Phase 1

Conditions

Duration of Labour

Treatments

Drug: Metoclopramide

Study type

Interventional

Funder types

Other

Identifiers

NCT05222646
AEFUTHA/16/07/2020.4/11/2020

Details and patient eligibility

About

BACKGROUND Prolonged labour can lead to increased maternal and neonatal mortality and morbidity. The risk for complications of prolonged labour is more in poor resource settings. Active management of labour has been shown to decrease the occurrence of prolonged labour. Administering antispasmodics during labour could also lead to faster and more effective dilatation of the cervix. As the evidence to support this is still largely anecdotal around the world, there is a need to conduct clinical trials so as to obtain a valid answer.

Full description

BACKGROUND Prolonged labour can lead to increased maternal and neonatal mortality and morbidity. The risk for complications of prolonged labour is more in poor resource settings. Active management of labour has been shown to decrease the occurrence of prolonged labour. Administering antispasmodics during labour could also lead to faster and more effective dilatation of the cervix. As the evidence to support this is still largely anecdotal around the world, there is a need to conduct clinical trials so as to obtain a valid answer.

OBJECTIVE This study is designed to compare the effectiveness of metoclopramide versus hyoscine butyl bromide in shortening the duration of the first stage of labour in Abakaliki.

Methods: This would be an equivalence randomized, double-blinded, placebo-controlled trial among nulliparous women in labour Abakaliki to determine the effectiveness of intramuscular Metoclopramide versus intramuscular Hyoscine bromide in shortening the duration of the first stage of labour. One arm will receive a single dose of 10mg of Metoclopramide intramuscularly, another will receive 20 mg of Hyoscine bromide, the third am will receive 1 ml of sterile water(placebo) intramuscularly. The data obtained will be analysed using Statistical Package for Social Science (IBM SPSS) software (version 20, Chicago II, USA) and the intention to treat the concept. Continuous variables would be presented as mean and standard deviation (Mean ± 2SD), while categorical variables would be presented as numbers and percentages. Logistic regression will also be applied where applicable. A difference with a P-value of ≤ 0.05 will be taken to be statistically significant.

Results: The results will be presented in tables from where conclusions will be drawn

CONCLUSION KEYWORD Prolonged labour, Metoclopramide, Hyoscine Bromide, the active phase of labour

Enrollment

150 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. All nullipara who gave consent

Exclusion criteria

  1. those who refused consent

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

150 participants in 2 patient groups

Metoclopramide group
Active Comparator group
Description:
They will be receiving10mg of Metoclopramide intramuscularly
Treatment:
Drug: Metoclopramide
Hyoscine bromide group
Active Comparator group
Description:
They will be receiving 20 mg of Hyoscine bromide
Treatment:
Drug: Metoclopramide

Trial contacts and locations

1

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Central trial contact

UGOJI DR DARLINGTON-PETER, PART 1; UWAKWE DR EMMANUEL CHIJIOKE, PART 1

Data sourced from clinicaltrials.gov

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