Skip to content

Uterotonic Efficacy of Oxytocin 2.5 Versus 10 Units During Caesarean Section at Mulago Hospital

Uterotonic Efficacy of Oxytocin 2.5 Versus 10 Units During Caesarean Section at Mulago Hospital; Adouble Blinded Clinical Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01726478
Enrollment
386
Registered
2012-11-15
Start date
2011-02-28
Completion date
2011-04-30
Last updated
2012-11-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adverse Effect of Oxytocic Drugs, Inappropriate Dose of Drug Administered, Uterine Hemorrhage

Keywords

Oxytocin, Uterine tone, Mulago Hospital, Dose, Side effects

Brief summary

The purpose of the study was to determine whether 2.5 international units of oxytocin gives adequate uterine tone and is safe as compared to 10 international units of oxytocin following caesarean section delivery at Mulago hospital.

Interventions

DRUG2.5 units Oxytocin

Administration of 2.5 units of oxytocin after clamping of umbilical cord

DRUG10 units Oxytocin

Administration of 10 units of oxytocin after clamping of umbilical cord

Sponsors

Faculty of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* ASA I (Healthy patient with no systemic disease) or II ( mild to moderate systemic disease) * Age between 18 to 40 years * Singleton pregnancies

Exclusion criteria

* • Allergy to oxytocin * Ruptured uterus * Significant obstetric disease (including Pregnancy induced Hypertension, Eclampsia,) * Known risk factors for postpartum haemorrhage or uterine atony * Inherited or acquired coagulation disorder * History of post partum haemorrhage

Design outcomes

Primary

MeasureTime frameDescription
Uterine tone adequacy2 minutesThe primary outcome was the assessment of either adequate or inadequate Uterine tone at various times after administration of initial oxytocin dose

Secondary

MeasureTime frameDescription
Intraoperative blood loss24 hoursBlood loss was estimated by measuring the amount in the suction bottles and weighing of the mops. The patients were followed up for any occurrence of postpartum haemorrhage for the next 24 hours after surgery.

Countries

Uganda

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026