MedPath

Intrauterine contraception among postpartum women in Uganda

Phase 3
Conditions
Fertility-female
Registration Number
PACTR201910683607569
Lead Sponsor
Makerere Unversity
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
232
Inclusion Criteria

•Postpartum women who will be willing to be followed up and give informed consent

Exclusion Criteria

•Intrapartum chorioamnionitis (defined as maternal fever >100.4 and two of the following conditions: Maternal leukocytosis (greater than 15,000 cells/cubic millimeter), Maternal tachycardia (greater than 100 beats/minute), Fetal tachycardia (greater than 160 beats/minute), Uterine tenderness, Foul odor of the amniotic fluid
•Postpartum Hemorrhage (defined as >500cc EBL for spontaneous vaginal delivery or >1000cc for cesarean delivery)
•Congenital or acquired uterine anomaly including fibroids if they distort the uterine cavity
•Acute liver disease or liver tumor
•Hypersensitivity to any component of the product
•Known or suspected carcinoma of the breast
•Current breast cancer or breast cancer within the past 5 years
•Decompensated cirrhosis or a liver tumor
•Known or suspected uterine or cervical neoplasia or unresolved, abnormal pap smear
•Unexplained vaginal bleeding prior to pregnancy

Study & Design

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