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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01958424
Other study ID # MMC-16092013-CTIL
Secondary ID
Status Completed
Phase N/A
First received October 6, 2013
Last updated May 10, 2016
Start date April 2014
Est. completion date December 2014

Study information

Verified date October 2013
Source Meir Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ethics Commission
Study type Observational

Clinical Trial Summary

The purpose of this study is to examine the effect of metabolic syndrome in over-weight women on IVF treatment outcomes.


Description:

This porpuse of the study is to examine the physiology of CRP during the IVF cycle in and to evaluated the effect of CRP in patient with and without metabolic syndrome on IVF outcomes


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- women undergoing ivf treatment

Exclusion Criteria:

- inflammatory disease

- acute conditions

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Sapir Medical Center, Meir Hospital Kfar-Saba

Sponsors (1)

Lead Sponsor Collaborator
Meir Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary success or failure of ivf treatment success or failure of a treatment will be determined by beta-Human chorionic gonadotropin test, number of oocyte retrieved or fertilized and embryos quality. within 1 year from intiation of ivf treatment No
Secondary blood levels of C-reactive protein within 1 year from initiation of ivf treatment No
Secondary follicle liquid levels of C-reactive protein within 1 year from initiation of ivf treatment No
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