The Telomere System in Cord Blood and in the Placenta in High Risk Pregnancies
This study is ongoing, but not recruiting participants.
Sponsor:
Meir Medical Center
Information provided by:
Meir Medical Center
ClinicalTrials.gov Identifier:
NCT01384136
First received: June 27, 2011
Last updated: NA
Last verified: June 2011
History: No changes posted
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Purpose
The telomere system stabilizes the chromosomes. Telomeres are shortened during senescence, in cases of genetic instability and secondary to stress.
The investigators aim is to study the telomere system in cord blood and in the placenta immediately after the delivery in pregnancies defined as high risk pregnancies following sterss events such as placental insufficiency, preeclampsia, diabetes.
The investigators intend to compare the telomere system in maternal blood to cord blood and to placental biopsies and to study the influence of different stressogenes on this system.
| Condition |
|---|
|
Telomere Length Mechanisms of Telomter Homeostasis High Risk Pregnancies |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Cross-Sectional |
| Official Title: | The Telomere System in Cord Blood and in the Placenta in High Risk Pregnancies |
Further study details as provided by Meir Medical Center:
| Estimated Enrollment: | 100 |
| Study Start Date: | June 2011 |
| Estimated Study Completion Date: | June 2015 |
| Estimated Primary Completion Date: | June 2015 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
| High risk pregnancy |
| /Control - Normal low risk pregnancies |
Eligibility| Ages Eligible for Study: | 18 Years to 45 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Study Population
High risk pregnancies, third trimester, after the delivery/
Criteria
Inclusion Criteria:
- Third trimester post delivery
- Intrauterine growth restriction
- Preeclampsia
- Diabetes
- Control - low risk normal pregnancies
Exclusion Criteria:
- Patients who do not want to participate
- Known HIV or Hepatitis
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Tal Biron-Shental, Meir Medical Center, Kfar Saba, Israel |
| ClinicalTrials.gov Identifier: | NCT01384136 History of Changes |
| Other Study ID Numbers: | 036-2011 MMC |
| Study First Received: | June 27, 2011 |
| Last Updated: | June 27, 2011 |
| Health Authority: | Internal Review Board - Helsinki Committee,Meir Medical Center Kfar Saba, Israel':' Israel: The Israel National Institute for Health Policy Research and Health Services Research |
ClinicalTrials.gov processed this record on May 16, 2013