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Clinical Trials/NCT02383537
NCT02383537
Unknown
Not Applicable

Biological Changes in the Adipose Tissue (RNA Profile) Among Pregnant Women With Diabetes

Hadassah Medical Organization0 sites150 target enrollmentApril 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pregnancy
Sponsor
Hadassah Medical Organization
Enrollment
150
Primary Endpoint
miRNA profiling
Last Updated
9 years ago

Overview

Brief Summary

The aim of the research is to study the effect of miRNA, fat tissue and insulin resistance on the pathophysiology of diabetes during pregnancy. During the study fat tissue, Umbilical cord blood, placenta tissue and subcutaneous fat will be taken from pregnant diabetic woman over going a C-section. Healthy pregnant women will serve as a control group.

Detailed Description

The aim of the research is to study the effect of miRNA, fat tissue and insulin resistance on the pathophysiology of diabetes during pregnancy. During the study: 1. fat tissue, Umbilical cord blood, placenta tissue and subcutaneous fat will be taken from pregnant diabetic woman over going a C-section. 2. Bloods will be analyzed for insulin, c-peptide, glucose and fat profile 3. Placenta and fat tissue will be analyzed for miRNA and total RNA 4. Clinical and anthropometric measurements will be taken from the mother 5. Placenta status will be taken

Registry
clinicaltrials.gov
Start Date
April 2017
End Date
February 2020
Last Updated
9 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age 18-45
  • signed consent form
  • going through an elective C-section
  • reference group: healthy women with no background illness

Exclusion Criteria

  • \<18 or \>45
  • chronic illness that may effect the outcome
  • polypharmacy

Outcomes

Primary Outcomes

miRNA profiling

Time Frame: samles are taken during C-section samples will be analyzed after completion of collection

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