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

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

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015090423887N1
Enrollment
60
Registered
2015-11-10
Start date
2014-03-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

preeclampsia. Gestational [pregnancy-induced] hypertension with significant proteinuria

Interventions

Intervention 1: In the intervention group, 3 and 24 hours after newborn birth, 70 mg of silymarin is to be orally administered to mother. Intervention 2: In the control group, 3 and 24 hours after bir
Treatment - Drugs
In the intervention group, 3 and 24 hours after newborn birth, 70 mg of silymarin is to be orally administered to mother.
In the control group, 3 and 24 hours after birth, placebo is to be administered to the mother.

Sponsors

Shahrekord University Of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 30 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Platlet count. Timepoint: 0,12,36 and 60 hours after intervention. Method of measurement: count in mm3.;Blood pressure. Timepoint: q 3 hours in study. Method of measurement: mmHg.;Liver enzyme. Timepoint: before and 12,36 and 60 hours after trial. Method of measurement: labratoary kit.

Secondary

MeasureTime frame
Number of blood pressure crisis in study. Timepoint: q 3 hours. Method of measurement: bp >160/110 mmhg.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Sepide Miraj

Shahrekord University Of Medical Sciences

miraj@skums.ac.ir+98 38 3222 0016

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026