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Clinical Trials/IRCT20221108056440N1
IRCT20221108056440N1
Recruiting
Phase 3

Comparison of the Effectiveness of l_arginine plus aspirin with aspirin alone in preventing adverse outcomes in pregnant women at high risk of preeclampsia

Kashan University of Medical Sciences0 sites90 target enrollmentStarted: TBDLast updated:

Overview

Phase
Phase 3
Status
Recruiting
Enrollment
90

Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
no limit to no limit (—)
Sex
Female

Inclusion Criteria

  • Pregnant women who are at high risk for preeclampsia
  • Pregnant women with a gestational age between 14 and 28 weeks of pregnancy
  • Previous history of pre\-eclampsia in the individual or first degree relatives of the individual's sister or mother
  • Women with a history of chronic hypertension
  • Body mass index greater than 30
  • Multiple pregnancy
  • Lipid disorders

Exclusion Criteria

  • Drug sensitivity to L\-arginine
  • Drug sensitivity to aspirin

Investigators

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