Effect of Infant Placement on Iron Stores in Infancy: A Pilot Study

December 30, 2008 updated by: Davison, James, D.O.

The Effect of Infant Placement at Delivery on Iron Stores in Early Infancy: A Pilot Study

This is a pilot study designed to assess the safety of placing an infant on the mother's abdomen at the time of delivery, prior to clamping the umbilical cord and the effect of placing the infant on the mother's abdomen on the infant's iron stores. It is possible that placing the infant on the mother's abdomen (above the placenta) may lower the infant's iron stores during early infancy.

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

30

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • healthy pregnant women
  • 37 - 42 weeks of gestation
  • vaginal delivery
  • prenatal care initiated prior to 20 weeks of gestation

Exclusion Criteria:

  • maternal diabetes
  • intrauterine growth restriction
  • hypertensive disorders of pregnancy
  • chronic hypertension requiring medical therapy
  • Apgar score less than 7 at 5 minutes
  • unusual bleeding prior to delivery
  • alloimmunization
  • maternal hemoglobinopathy
  • need for immediate infant resuscitation preventing adherence to protocol

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: perineum
infants maintained at the level of the perineum until umbilical cord clamping
infants maintained at the level of the perineum until umbilical cord clamping
Experimental: abdomen
infants placed on the maternal abdomen prior to cord clamping
infants placed on the maternal abdomen prior to umbilical cord clamping

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
serum ferritin level at 4 months of age
Time Frame: 4 months
4 months

Secondary Outcome Measures

Outcome Measure
Time Frame
blood parameters (hemoglobin and hematocrit)
Time Frame: 2 months and 4 months
2 months and 4 months
serum ferritin at 2 months
Time Frame: 2 months
2 months
blood parameters (hemoglobin and hematocrit) at 24 hrs of age
Time Frame: 24 hrs.
24 hrs.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: James M Davison, DO, Warren General Hospital
  • Principal Investigator: Sunny A Thomas, MD, Warren General Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2008

Primary Completion (Actual)

December 1, 2008

Study Completion (Anticipated)

April 1, 2009

Study Registration Dates

First Submitted

May 7, 2008

First Submitted That Met QC Criteria

May 8, 2008

First Posted (Estimate)

May 9, 2008

Study Record Updates

Last Update Posted (Estimate)

December 31, 2008

Last Update Submitted That Met QC Criteria

December 30, 2008

Last Verified

December 1, 2008

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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