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The Association Between Severity of Hypertensive Disorder During Pregnancy and Endothelial Dysfunction

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Clalit Health Services

Status

Unknown

Conditions

Endothelial Dysfunction

Treatments

Other: Observational only

Study type

Observational

Funder types

Other

Identifiers

NCT02334839
0206-14

Details and patient eligibility

About

Preeclampsia toxemia (PET) is a pregnancy related complication that is usually expressed as new onset hypertension and proteinuria after 20 weeks of gestation. scarce data exists regarding the effectiveness of PAT plethysmography use in women with PET and whether adverse results are found compared to healthy gravidas. Thus, we aimed to assess endothelial function using PAT plethysmography in women with PET and compare their results to both healthy gravidas and those with only gestational hypertension.

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Full description

Preeclampsia toxemia (PET) is a pregnancy related complication that is usually expressed as new onset hypertension and proteinuria after 20 weeks of gestation. Although the exact pathophysiology is unclear, it's related to abnormal placentation and subsequent vascular pathology. Endothelial dysfunction was found to play a significant role in the risk of cardiovascular event in general. Moreover, few studies found a relation between endothelial dysfunction and PET. There are several methods for the assessment of endothelial function, with Peripheral Artery Tone (PAT) plethysmography being an emerging non-invasive promising technique. However, scarce data exists regarding the effectiveness of PAT plethysmography use in women with PET and whether adverse results are found compared to healthy gravidas.

Thus, we aimed to assess endothelial function using PAT plethysmography in women with PET and compare their results to both healthy gravidas and those with only gestational hypertension.

Enrollment

150 estimated patients

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Maternal age 18-40 years old
  2. 27 and above weeks of gestation
  3. Singleton pregnancy
  4. Agreed to participate in the study and signed on informed consent form.

Exclusion criteria

  1. Known ischemic heart disease or angina pectoris
  2. Active smoker
  3. Dyslipidemia, chronic hypertension. Renal disease, diabetes mellitus (gestational or pregestational)
  4. Active treatment with anti-hypertensive medication, anti-aggregation medication or lipid lowering agents.

Trial design

150 participants in 3 patient groups

Preeclampsia
Description:
women with diagnosed preeclampsia
Treatment:
Other: Observational only
gestational hypertension
Description:
women with diagnosed gestational hypertension without preeclampsia
Treatment:
Other: Observational only
healthy
Description:
women without gestational hypertension or preeclampsia
Treatment:
Other: Observational only

Trial contacts and locations

1

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Central trial contact

Liran Hiersch

Data sourced from clinicaltrials.gov

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