Clinical Trials Directory

Trials / Terminated

TerminatedNCT01193192

A Retrospective Analysis of Neevo® and NeevoDHA® Compared to a Standard Prenatal Vitamin in Anemia During Pregnancy

Status
Terminated
Phase
Study type
Observational
Enrollment
30 (actual)
Sponsor
Pamlab, L.L.C. · Industry
Sex
Female
Age
21 Years – 39 Years
Healthy volunteers
Accepted

Summary

This study is a multi-site, retrospective chart review to determine the effect of Neevo® or NeevoDHA® (with higher folate and B12) versus standard prenatal vitamins on hemoglobin (Hgb) levels in pregnant women throughout the course of pregnancy. Neevo® is a prescription medical food indicated for the dietary management of women under a doctor's care who face high risk pregnancies, older overactive bladder (OB) patients and patients unable to fully metabolize folic acid. Data will be collected from existing patient charts of subjects administered Neevo® or NeevoDHA® daily compared to subjects administered a prenatal vitamin daily.

Conditions

Interventions

TypeNameDescription
OTHERNeevo®A prenatal "medical food" - analogous to a prenatal vitamin but containing L-methylfolate in addition to folic acid
OTHERPrenatal vitaminsfor inclusion in the Control Group, prenatal vitamins must have contained ≤1mg folic acid, 27 - 35mg iron, and ≤12mcg vitamin B12.

Timeline

Start date
2010-07-01
Primary completion
2010-11-01
Completion
2010-11-01
First posted
2010-09-01
Last updated
2011-11-23

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01193192. Inclusion in this directory is not an endorsement.