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

Sponsor
Uwakwe Emmanuel Chijioke (Other)
Overall Status
Recruiting
CT.gov ID
NCT05222646
Collaborator
(none)
150
1
2
7.9
19.1

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
Phase 1

Detailed 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

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Will receive single dose of 10mg of Metoclopramide intramuscularlyWill receive single dose of 10mg of Metoclopramide intramuscularly
Masking:
Double (Participant, Investigator)
Masking Description:
Will receive 20 mg of Hyoscine bromide,
Primary Purpose:
Prevention
Official Title:
Metoclopramide Versus Hyoscine Butylbromide in Shortening Duration of the First Stage of Labor Among Nulliparous Women in Abakaliki
Actual Study Start Date :
Jan 3, 2022
Anticipated Primary Completion Date :
Aug 3, 2022
Anticipated Study Completion Date :
Aug 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Metoclopramide group

They will be receiving10mg of Metoclopramide intramuscularly

Drug: Metoclopramide
Will receive single dose of 10mg of Metoclopramide intramuscularly
Other Names:
  • Placebo
  • Active Comparator: Hyoscine bromide group

    They will be receiving 20 mg of Hyoscine bromide

    Drug: Metoclopramide
    Will receive single dose of 10mg of Metoclopramide intramuscularly
    Other Names:
  • Placebo
  • Outcome Measures

    Primary Outcome Measures

    1. Duration of first stage of labour [6 months]

      Duration of first stage of labour

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 45 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    1. All nullipara who gave consent
    Exclusion Criteria:
    1. those who refused consent

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 AEFUTHA Abakaliki Ebonyi Nigeria 234

    Sponsors and Collaborators

    • Uwakwe Emmanuel Chijioke

    Investigators

    • Principal Investigator: Uwakwe DR Emmanuel Chijioke, PART 1, Alex Ekwueme Federal University Teaching Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Uwakwe Emmanuel Chijioke, Principal Investigator, Alex Ekwueme Federal University Teaching Hospital
    ClinicalTrials.gov Identifier:
    NCT05222646
    Other Study ID Numbers:
    • AEFUTHA/16/07/2020.4/11/2020
    First Posted:
    Feb 3, 2022
    Last Update Posted:
    Feb 3, 2022
    Last Verified:
    Feb 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 3, 2022