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EFFECTS OF ANTENATAL ANTIHELMINTHIC TREATMENT ON PREGNANCY OUTCOMES IN UITH ILORIN: A RANDOMISED CONTROLLED TRIAL.

Not Applicable
Conditions
Helminthiasis
Pregnancy and Childbirth
Registration Number
PACTR202008475715326
Lead Sponsor
Dr Afusat Olabinjo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
176
Inclusion Criteria

•All consenting pregnant women with singleton foetus presenting between 14 and 26 weeks.

Exclusion Criteria

•Non consenting pregnant women.
•Patients with known hypersensitivity to benzimidazole.
•Baseline haemoglobin concentration less than 7g/dl.
•Patients with multiple gestations.
•Patients with sickle cell disease
•Patients with chronic kidney disease.
•Retroviral disease patients.
•Patients that may require blood transfusion during the course of pregnancy.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Maternal stool parasite density
Secondary Outcome Measures
NameTimeMethod
The secondary outcomes will be determined by maternal anaemia and neonatal birth weight, APGAR scores NICU admission and still birth.
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