Expired Study
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Chicago, Illinois 60637


Purpose:

Recurrent miscarriage is a prevalent reproductive problem that affects many couples who are trying to establish a family. This clinical study will evaluate the effectiveness of intravenous immunoglobulin (IVIG) in improving the live birth rate in couples who suffer from secondary recurrent miscarriage. This study will help in providing an answer to the question of whether IVIG is helpful in secondary recurrent miscarriage.


Study summary:

The purpose of this multi-center trial is to evaluate the efficacy of IVIG in improving the ongoing pregnancy (>20 weeks of gestation) rate in couples with unexplained secondary recurrent miscarriage, and; to characterize and compare pharmacokinetic and pharmacodynamic parameters for IVIG pre-conceptually and in the 1st and 2nd trimesters of pregnancy, so that an improved IVIG dosing strategy can be determined.


Criteria:

Inclusion Criteria: - Couple has a history of unexplained secondary recurrent miscarriage. - Most recent pregnancy occurred within one year of discontinuing contraception. Exclusion Criteria: - Maternal IgA deficiency - Maternal history of immunoglobulin hypersensitivity. - Maternal contraindication to pregnancy. - Evidence of active hepatitis or immunocompromised state in either partner. - Concomitant use of medication(s) for treatment of recurrent miscarriage, such as but not limited to progesterone, clomiphene citrate, acetylsalicylic acid, heparin, glucocorticoids or hCG injections.


NCT ID:

NCT00606905


Primary Contact:

Study Chair
Mary D Stephenson, MD, MSc
University of Chicago


Backup Contact:

N/A


Location Contact:

Chicago, Illinois 60637
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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