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Clinical Trials/IRCT2015090423887N1
IRCT2015090423887N1CompletedEarly Phase 1

Evaluation the effect of silimaryn in improvement of hepatic and platlet damage in severe preeclampsia

Shahrekord University Of Medical Sciences0 sites60 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Early Phase 1
Status
Completed
Enrollment
60

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20 years to 30 years (—)
Sex
Female

Inclusion Criteria

  • age between 20 and 30 years; BMI is to be 20 to 24;Gestational age is between 35 and 42 weeks at the time of termination of pregnancy; blood pressure before the termination of pregnancy is to be more than 90/140 mm Hg;The presence of Proteinuria in random urine samples before pregnancy termination; no history of hypertension, diabetes, kidney disease, Collagen vascular and other types of cardiovascular diseases; mother is supposed to be nulliparous; Singleton pregnancy not molar; termination of pregnancy is indicated By severe pre-eclampsia
  • Exclusion criteria:presence of preeclampsia in mother

Exclusion Criteria

  • Not provided

Investigators

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