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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03390010
Other study ID # Active management of labour
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date December 28, 2017
Est. completion date March 6, 2018

Study information

Verified date November 2022
Source Aljazeera Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Several treatment strategies are emplemented to prevent post delivery hemorage and decreasing maternal morbidity and mortality .


Description:

Many approved drugs are used in prophylaxis against postpartum hemorage from these medications are the (syntocinon combined with methergine ) that are known as active management of labour drugs . Moreover there is misotac , that also guards against postpartum hemorage . All these medications act in a different way to cause uterine contraction post delivery to prevent uterine atony . -Here we are comparing the additive value of misotac intrauterine to syntocinon and methergine in comparison to the usually used syntocinon plus methergine .


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date March 6, 2018
Est. primary completion date February 28, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 42 Years
Eligibility Inclusion Criteria: - • All patients included in this research were aged 18-42 years, pregnant 37 weeks till 42 weeks - no medical disorders with pregnancy e.g DM, HTN. All patients were subjected to full history taking, examination. Exclusion Criteria: - Exclusion Criteria: - The following patients were excluded , GA before 37 weeks or after 42 weeks , medical disorders with pregnancy eg. DM with pregnancy, HTN with pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Misoprostol + syntocinon and using extra uterotonic drugs when needed ; methergine
medical prophylaxis against postpartum atony and postpartum hemorage by giving misoprostol plus syntocinon and using extra uterotonic drugs when needed ; methergine, carboprost
Syntocinon and using extra uterotonic drugs when needed ; methergine carboprost
medical prophylaxis against postpartum atony and postpartum hemorage by giving syntocinon and using extra uterotonic drugs when needed ; methergine, carboprost

Locations

Country Name City State
Egypt Algazeerah Giza

Sponsors (2)

Lead Sponsor Collaborator
Aljazeera Hospital Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The number of participants who passed cesarean section without postpartum hemorage within 2 days post CS
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