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The Efficacy of Intermittent Versus Daily Oral Iron Supplementation in Anaemic Pregnant Women.

NCT05278793 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 58

Last updated 2022-03-14

No results posted yet for this study

Summary

In this study intermittent dosage of iron supplementation three times a week will be compared to daily dosage in anaemic pregnant women due to iron deficiency.

Conditions

Interventions

DRUG

Ferrous fumarate

Ferrous fumarate 200mg oral

Sponsors & Collaborators

  • dr. J.M. Munster, gynaecologist, principal investigator

    collaborator UNKNOWN

  • Martini Hospital Groningen

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-01-07
Primary Completion
2022-12-31
Completion
2022-12-31

Countries

  • Netherlands

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05278793 on ClinicalTrials.gov